(R)-(+)-1-苯基乙醇

  • ≥99%
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货号 (SKU) 包装规格 是否现货 价格 数量
P100878-1g
1g 现货 Stock Image
P100878-5g
5g 现货 Stock Image
P100878-10g
10g 现货 Stock Image
P100878-25g
25g 现货 Stock Image
P100878-100g
100g 现货 Stock Image
P100878-500g
500g 现货 Stock Image
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醇 (851) 非杂环砌块 (8211)

基本描述

别名 (R)-(+)-1-苯乙醇 | (R)-(+)-α-甲基苄醇 | (R)-1-苯基乙醇 | (R)-(+)-1-苯基乙醇
英文别名 (R)-(+)-1-Phenylethanol | (R)-(+)-sec-Phenethyl Alcohol | (R)-(+)-α-Methylbenzyl Alcohol
规格或纯度 ≥99%
英文名称 (R)-(+)-1-Phenylethanol
运输条件 常规运输
产品介绍

( R )-1-苯乙醇可通过乙苯在过氧化酶催化下的对映选择性羟基化制备。

It can be prepared from ethylbenzene via enantioselective hydroxylation of ethylbenzene catalyzed by peroxygenase enzyme.

AI解读

关联靶点(其它种属)

Sult1a1 Aryl sulfotransferase (136 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Triticum aestivum (1582 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

作用机制

作用机制 Action Type target ID Target Name Target Type Target Organism Binding Site Name 参考文献

名称和识别符

PubChem SID 488190841
分子类型 小分子
IUPAC Name (1R)-1-phenylethanol
INCHI InChI=1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3/t7-/m1/s1
InChi Key WAPNOHKVXSQRPX-SSDOTTSWSA-N
Canonical SMILES C[C@@H](O)c1ccccc1
Isomeric SMILES C[C@H](C1=CC=CC=C1)O
WGK Germany 3
PubChem CID 637516
UN Number 2937
分子量 122.16
Beilstein号 2039798
Reaxy-Rn 2039798

化学和物理性质

溶解性 Miscible with organic solvents and slightly miscible with water.
密度 1.01
折光率 1.526-1.528
闪点(℉) 185.0 °F
闪点(℃) 85℃
沸点 98°C
熔点 9-11°C
分子量 122.160 g/mol
XLogP3 1.400
氢键供体数Hydrogen Bond Donor Count 1
氢键受体数Hydrogen Bond Acceptor Count 1
可旋转键计数Rotatable Bond Count 1
精确质量Exact Mass 122.073 Da
单同位素质量Monoisotopic Mass 122.073 Da
拓扑极表面积Topological Polar Surface Area 20.200 Ų
重原子数Heavy Atom Count 9
形式电荷Formal Charge 0
复杂度Complexity 74.600
同位素原子数Isotope Atom Count 0
定义的原子立体中心计数Defined Atom Stereocenter Count 1
未定义的原子立体中心计数Undefined Atom Stereocenter Count 0
定义的键立体中心计数Defined Bond Stereocenter Count 0
未定义的键立体中心计数Undefined Bond Stereocenter Count 0
所有立体化学键的总数The total count of all stereochemical bonds 0
共价键合单元计数Covalently-Bonded Unit Count 1

安全和危险性(GHS)

一般危化品 一般危化品
象形图 GHS05,   GHS07
信号词 Danger
危险声明

H315: 引起皮肤刺激

H302: 吞食有害

H318: 造成严重的眼睛损伤

预防措施声明

P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。

P302+P352: 如皮肤沾染:用水充分清洗。

P321: 特殊处理(请参阅此标签上的...)。

P501: 将内容物/容器处理到。。。

P264: 处理后要彻底洗手。

P270: 使用本产品时,请勿进食、饮水或吸烟。

P362+P364: 脱掉沾污的衣服,清洗后方可重新使用。

P330: 漱口

P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。

P301+P317: 如果被吞咽:请寻求医疗帮助。

P305+P354+P338: 如果进入眼睛:立即用水冲洗几分钟。取下隐形眼镜(如果有的话),并且操作简单。继续冲洗。

P317: 寻求紧急医疗救助。

P332+P317: 如果出现皮肤刺激:请寻求医疗帮助。

WGK Germany 3
Reaxy-Rn 2039798
个人防护装备 Eyeshields,Faceshields,full-face respirator (US),Gloves,multi-purpose combination respirator cartridge (US),type ABEK (EN14387) respirator filter

技术规格说明书

Refractive index n20/D 1.525-1.529
Purity(GC) 99-100(%)
Specific Rotation [a]20/D 43-48(°)
Appearance(P100878) Colorless to Yellow Liquid
Infrared spectrum Conforms to Structure

质检证书(CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:

通过匹配包装上的批号来查找并下载产品的 COA,每批产品都进行了严格的验证,您可放心使用!

找到20个结果

批号(Lot Number) 证书类型 日期 货号
G2110355 分析证书 25-04-03 P100878
G2110353 分析证书 25-04-03 P100878
L2412494 分析证书 24-11-27 P100878
L2412493 分析证书 24-11-27 P100878
L2412492 分析证书 24-11-27 P100878
H2409393 分析证书 24-06-12 P100878
F2428493 分析证书 24-06-04 P100878
F2428495 分析证书 24-06-04 P100878
F2428494 分析证书 24-06-04 P100878
F2428492 分析证书 24-06-04 P100878
F2428491 分析证书 24-06-04 P100878
F2428490 分析证书 24-06-04 P100878
F2428489 分析证书 24-06-04 P100878
D1828175 分析证书 22-03-24 P100878
D1828174 分析证书 22-03-24 P100878
E2207041 分析证书 22-03-14 P100878
G2314153 分析证书 22-03-14 P100878
E2207040 分析证书 22-03-14 P100878
E2207039 分析证书 22-03-14 P100878
E2207038 分析证书 22-03-14 P100878

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此产品的引用文献

1. Miao Chen, Xiaole Li, Jinfan Li, Chunyan Liu, Ajuan Yu, Shusheng Zhang.  (2024)  Highly enantioseparation in membrane-supported one-dimensional metal–organic framework hollow nanotube array prepared via mussel-inspired chemistry.  SEPARATION AND PURIFICATION TECHNOLOGY,  331  (31): (125704).  [PMID:8363592] [10.1016/j.seppur.2023.125704]
2. Pan Jiang, Hongkun Li, Wei Liu, Yi Li, Baozong Li, Yonggang Yang.  (2021)  Silica covering driven intensity enhancement and handedness inversion of the CPL signals of the supramolecular assemblies.  NEW JOURNAL OF CHEMISTRY,  45  (20): (8986-8992).  [10.1039/D1NJ01327K]
3. Weican Wang, Ling Li, Xiaoda Wang, Ting Qiu, Jianhao Yang, Changshen Ye.  (2021)  Reaction kinetic studies on the immobilized-lipase catalyzed enzymatic resolution of 1-phenylethanol transesterification with ethyl butyrate.  BIOCATALYSIS AND BIOTRANSFORMATION,  [10.1080/10242422.2020.1855150]
4. Zhang Yajuan, Duan Yajuan, Zhong Lingli, Li Zhoukun, Cui Zhongli, Huang Yan.  (2020)  Characterization of a novel aldo-keto reductase with anti-Prelog stereospecificity from Corallococcus sp. EGB.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  146  (36).  [PMID:31887378] [10.1016/j.ijbiomac.2019.12.214]
5. Dun Deng, Yun Zhang, Aijun Sun, Yunfeng Hu.  (2016)  Enantio-selective preparation of (S)-1-phenylethanol by a novel marine GDSL lipase MT6 with reverse stereo-selectivity.  CHINESE JOURNAL OF CATALYSIS,  37  (1966).  [10.1016/S1872-2067(16)62505-6]

参考文献

1. Sachiko Sugimoto,Amira Samir Wanas,Tsutomu Mizuta,Katsuyoshi Matsunami,Mohamed Salah Kamel,Hideaki Otsuka.  (2014-12-03)  Structure elucidation of secondary metabolites isolated from the leaves of Ixora undulate and their inhibitory activity toward advanced glycation end-products formation..  Phytochemistry,  108  (189-195).  [PMID:25456209]
2. Miao Chen, Xiaole Li, Jinfan Li, Chunyan Liu, Ajuan Yu, Shusheng Zhang.  (2024)  Highly enantioseparation in membrane-supported one-dimensional metal–organic framework hollow nanotube array prepared via mussel-inspired chemistry.  SEPARATION AND PURIFICATION TECHNOLOGY,  331  (31): (125704).  [PMID:8363592] [10.1016/j.seppur.2023.125704]
3. Pan Jiang, Hongkun Li, Wei Liu, Yi Li, Baozong Li, Yonggang Yang.  (2021)  Silica covering driven intensity enhancement and handedness inversion of the CPL signals of the supramolecular assemblies.  NEW JOURNAL OF CHEMISTRY,  45  (20): (8986-8992).  [10.1039/D1NJ01327K]
4. Weican Wang, Ling Li, Xiaoda Wang, Ting Qiu, Jianhao Yang, Changshen Ye.  (2021)  Reaction kinetic studies on the immobilized-lipase catalyzed enzymatic resolution of 1-phenylethanol transesterification with ethyl butyrate.  BIOCATALYSIS AND BIOTRANSFORMATION,  [10.1080/10242422.2020.1855150]
5. Zhang Yajuan, Duan Yajuan, Zhong Lingli, Li Zhoukun, Cui Zhongli, Huang Yan.  (2020)  Characterization of a novel aldo-keto reductase with anti-Prelog stereospecificity from Corallococcus sp. EGB.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  146  (36).  [PMID:31887378] [10.1016/j.ijbiomac.2019.12.214]
6. Dun Deng, Yun Zhang, Aijun Sun, Yunfeng Hu.  (2016)  Enantio-selective preparation of (S)-1-phenylethanol by a novel marine GDSL lipase MT6 with reverse stereo-selectivity.  CHINESE JOURNAL OF CATALYSIS,  37  (1966).  [10.1016/S1872-2067(16)62505-6]

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