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Merck
CN

155322

Sigma-Aldrich

反-苯乙烯乙酸

greener alternative

96%

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别名:
4-苯基-3-丁烯酸
线性分子式:
C6H5CH=CHCH2CO2H
CAS号:
分子量:
162.19
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

96%

环保替代产品得分

old score: 22
new score: 3
Find out more about DOZN™ Scoring

环保替代产品特性

Atom Economy
Design for Energy Efficiency
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

84-86 °C (lit.)

环保替代产品分类

SMILES字符串

OC(=O)C\C=C\c1ccccc1

InChI

1S/C10H10O2/c11-10(12)8-4-7-9-5-2-1-3-6-9/h1-7H,8H2,(H,11,12)/b7-4+

InChI key

PSCXFXNEYIHJST-QPJJXVBHSA-N

一般描述

已对反式苯乙烯乙酸氢键系统的偏振红外光谱进行研究
我们竭诚为您带来满足绿色替代产品四大类别要求的替代产品。本品属于重新设计产品类别,在“原子经济”、“设计要有能效”和“使用可再生的原料”绿色化学原则方面取得了重大进步。 点击此处查看其DOZN记分卡。

应用

反式苯乙烯乙酸(4-苯基-3-丁烯酸)作为基于机制的肽酰甘氨酸 α 抑制剂-羟基化单加氧酶

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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J Scognamiglio et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50 Suppl 2, S120-S123 (2011-10-29)
A toxicologic and dermatologic review of 4-phenyl-3-buten-2-ol when used as a fragrance ingredient is presented. 4-Phenyl-3-buten-2-ol is a member of the fragrance structural group Aryl Alkyl Alcohols and is a secondary alcohol. The AAAs are a structurally diverse class of
W J Driscoll et al.
Biochemistry, 39(27), 8007-8016 (2000-07-13)
The bifunctional enzyme peptidylglycine-alpha-amidating monooxygenase mediates the conversion of C-terminal glycine-extended peptides to their active alpha-amidated products. Peptidylglycine-alpha-hydroxylating monooxygenase (PHM, EC 1.14.17. 3) catalyzes the first reaction in this two-step process. The olefinic compound 4-phenyl-3-butenoic acid (PBA) is the most
Yuan-Ning Cao et al.
Regulatory peptides, 113(1-3), 109-114 (2003-04-11)
Human adrenomedullin (hAM) is an endogenous peptide that has potent vasodilator activity. Mature AM is biosynthesized from its intermediate form, glycine-extended AM (AM-gly), by carboxy-terminal amidation. AM-gly is generally considered to be biologically inactive but is a major molecular form
David J Merkler et al.
Biochemistry, 43(39), 12667-12674 (2004-09-29)
Oleamide is an endogenous sleep-inducing lipid that has been isolated from the cerebrospinal fluid of sleep-deprived mammals. Oleamide is the best-understood member of the primary fatty acid amide family. One key unanswered question regarding oleamide and all other primary acid
Emma Langella et al.
ChemMedChem, 5(9), 1568-1576 (2010-08-18)
Specific inhibition of the copper-containing peptidylglycine alpha-hydroxylating monooxygenase (PHM), which catalyzes the post-translational modification of peptides involved in carcinogenesis and tumor progression, constitutes a new approach for combating cancer. We carried out a structure-activity study of new compounds derived from

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