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1822-46-4

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1822-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1822-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1822-46:
(6*1)+(5*8)+(4*2)+(3*2)+(2*4)+(1*6)=74
74 % 10 = 4
So 1822-46-4 is a valid CAS Registry Number.

1822-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name di(pyrrolidine-1)-1,2 propane

1.2 Other means of identification

Product number -
Other names 1,2-bis-(pyrrolidino)-propan

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:1822-46-4 SDS

1822-46-4Downstream Products

1822-46-4Relevant articles and documents

N-Alkylation d'amines en catalyse homogene. Synthese de mono- et de diamines cycliques

Bitsi, G.,Schleiffer, E.,Antoni, F.,Jenner, G.

, p. 343 - 352 (2007/10/02)

Ruthenium compounds are appropriate catalysts in the N-alkylation of amines.The synthesis of N-alkylated cyclic amines from a cyclic amine and an alcohol or via the condensation between a diol and a primary amine are described.The reaction with cyclic amines is highly selective, especially in the presence of a phosphine, making it a high yielding preparative procedure.The catalytic condensation between cyclic amines and diols yields either an aminoalcohol (A) or a bicyclic diamine (B).The temperature, the presence of phosphine, and the ratio of amine to diol are decisive in directing the reaction toward A or B.The proposed mechanism involves the dehydrogenation of the alcohol followed by attack of the amine on the aldehyde intermediate.

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