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2156-71-0

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2156-71-0 Usage

General Description

NISTC2156710, also known as 2-butanol, is a chemical compound with the molecular formula C4H10O. It is a colorless liquid with a strong, sweet odor, and is commonly used as a solvent and in the production of various chemicals. 2-butanol is flammable and can be harmful if inhaled, ingested, or absorbed through the skin. It is also a respiratory and skin irritant and should be handled with care. In addition, 2-butanol is known to be toxic to aquatic organisms and should be disposed of properly to prevent environmental contamination. Overall, NISTC2156710 is a versatile chemical with various industrial applications, but proper safety precautions should be taken when handling and using it.

Check Digit Verification of cas no

The CAS Registry Mumber 2156-71-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2156-71:
(6*2)+(5*1)+(4*5)+(3*6)+(2*7)+(1*1)=70
70 % 10 = 0
So 2156-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H10ClN/c6-7-4-2-1-3-5-7/h1-5H2

2156-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloropiperidine

1.2 Other means of identification

Product number -
Other names 1-Chlor-piperidin

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:2156-71-0 SDS

2156-71-0Relevant articles and documents

Structure-activity considerations in kinetics and mechanism of chlorine exchange between chloramine-T and secondary amines

Dannan,Hussain,Crooks,Dittert

, p. 657 - 660 (2007/10/02)

To study the mechanism of N-chlorination of secondary amines by chloramine-T, the kinetics of the reactions of some aromatic-substituted analogues of N-chlorobenzenesulfonamide with various secondary amines were determined. The importance of amine basicity and reactivity of the N-Cl bond of the N-chlorobenzenesulfonamide was also assessed. The results indicate that a mechanism involving the un-ionized species of both reactants (i.e., a molecular mechanism), rather than an ionic mechanism, is operating and that the reaction most likely proceeds via a six-membered-ring transition state that incorporates a water molecule.

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