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62922-45-6

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62922-45-6 Usage

Uses

2,5-Dichloroamylamine hydrochloride may be used in chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 62922-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,2 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62922-45:
(7*6)+(6*2)+(5*9)+(4*2)+(3*2)+(2*4)+(1*5)=126
126 % 10 = 6
So 62922-45-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H11Cl2N.ClH/c6-3-1-2-5(7)4-8;/h5H,1-4,8H2;1H

62922-45-6 Well-known Company Product Price

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  • Aldrich

  • (279110)  2,5-Dichloroamylaminehydrochloride  technical grade, 95%

  • 62922-45-6

  • 279110-100G

  • 1,590.03CNY

  • Detail

62922-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-DICHLOROPENTYLAMINE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names 2,5-Dichloropentylamine HCl

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:62922-45-6 SDS

62922-45-6Relevant articles and documents

Bis(β-hydroxyethylthio)-C1 -C4 -alkylamines

-

, (2008/06/13)

This application relates to intermediates useful for the preparation of fiber-reactive dyes, said intermediates having the formulae STR1 in which B is a --(CH2)n -- or --O--(CH2)n -- radical, where n is 1 to 6; Q is selected from the group consisting of hydrogen, C1 -C4 alkyl, C1 -C4 alkoxy, halogen, carboxyl and sulfo; and A is an amino substituent of the formula STR2 and Z and Z', independently of one another, are β-sulfatoethyl, β-thiosulfatoethyl, β-phosphatoethyl, β-acyloxyethyl, β-haloethyl or vinyl.

Preparation of N-alkenyl-2-aminomethyl-pyrrolidines

-

, (2008/06/13)

An N-alkenyl-2-aminomethyl-pyrrolidine is prepared by firstly reacting tetrahydrofurfurylamine with gaseous hydrochloric acid and thionyl chloride to produce 2,5 dichloropentylamine hydrochloride. This is acetylized, possibly by acetyl chloride in dichloroethane in the presence of triethylamine, into N-acetyl-2,5-dichloropentylamine which is condensed with an alkenylamine into an N-alkenyl-2-acetylaminomethyl pyrrolidine from which the acetyl group is separated, for example by boiling with concentrated hydrochloric acid.

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