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23451-67-4

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23451-67-4 Usage

Physical state

Clear, colorless liquid

Odor

Pungent

Flammability

Highly flammable

Health hazards

Causes irritation to skin, eyes, and respiratory system

Precautions

Handle and store with caution to minimize risk to human health and environment

Uses

a. Solvent in organic synthesis
b. Intermediate in the production of pharmaceuticals
c. Intermediate in the production of pesticides
d. Intermediate in the production of other fine chemicals

Check Digit Verification of cas no

The CAS Registry Mumber 23451-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,5 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23451-67:
(7*2)+(6*3)+(5*4)+(4*5)+(3*1)+(2*6)+(1*7)=94
94 % 10 = 4
So 23451-67-4 is a valid CAS Registry Number.

23451-67-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-3-ethylsulfanylpropan-2-ol

1.2 Other means of identification

Product number -
Other names 1-chloro-3-ethylsulfanyl-propan-2-ol

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:23451-67-4 SDS

23451-67-4Relevant articles and documents

(Bromodimethyl)sulfonium bromide-mediated thiolysis of epoxides: An easy access to -hydroxy sulfides and benzoxathiepinones in solvent-free conditions

Shailaja,Manjula,Rao, B. Vittal

experimental part, p. 3629 - 3639 (2011/02/22)

A mild, rapid and highly regioselective opening of epoxides by mercaptans to bη-hydroxy sulfides and benzoxathiepinones has been achieved in excellent yields, using catalytic amount of (bromodimethyl)sulfonium bromide in solvent free reaction conditions.

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