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Benzenemethanethiol, α-ethyl-, also known as 2-ethylbenzenemethanethiol or α-ethylbenzyl mercaptan, is an organic compound with the chemical formula C9H12S. It is a colorless to pale yellow liquid with a strong, unpleasant odor. Benzenemethanethiol, a-ethyl- is primarily used as a synthetic intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a flavoring agent in the food and beverage industry, contributing to the aroma of various products. Due to its reactive nature, it is essential to handle Benzenemethanethiol, α-ethyl- with proper safety measures to avoid potential health hazards and environmental contamination.

76877-93-5

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76877-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76877-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,7 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76877-93:
(7*7)+(6*6)+(5*8)+(4*7)+(3*7)+(2*9)+(1*3)=195
195 % 10 = 5
So 76877-93-5 is a valid CAS Registry Number.

76877-93-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-mercapto-1-phenylpropane

1.2 Other means of identification

Product number -
Other names phenylpropyl mercaptan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76877-93-5 SDS

76877-93-5Relevant academic research and scientific papers

Stereoelectronic effects and chiral recognition, II: Kinetic and thermodynamic control in the formation of chiral thioacetals and chiral thioethers

Noe, Christian R.,Knollmueller, Max,Ziebarth-Schroth, Irene,Letschnig, Marion

, p. 1009 - 1013 (2007/10/03)

The ratio of diastereomers obtained from chiral thiols 2 was shown to be time-dependent both in thioacetal formation with lactol 1 (diastereomers 3/4) and in 1,4-addition to nitrostyrene 5 (diastereomers 6/7, 8/9). An interpretation based on stereoelectronic effects is presented to explain the similarity of the reaction pathways in both reactions. VCH Verlagsgesellschaft mbH, 1996.

Direct Conversion of Alcohols into Thiols

Nishio, Takehiko

, p. 1113 - 1118 (2007/10/02)

A simple one-pot reaction between alcohols and 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide (Lawesson's reagent, LR) affords the corresponding thiols, accompanied by dehydration products, alkenes.Treatment of acyclic 1,4-diols with LR gives the 1,3-dienes. o-(Dihydroxymethyl)benzene derivatives yield the 1,3-dihydrobenzothiophenes when treated with LR.

A Novel Transformation of Alcohols to Thiols

Nishio, Takehiko

, p. 205 - 206 (2007/10/02)

Treatment of alcohols with 2,4-bis(p-methoxyphenyl)-1,3-dithiaphosphetane-2,4-disulphide (Lawesson reagent) gave the corresponding thiols.

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