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cis-3,4-dibromopyrrolidine hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77484-76-5

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77484-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77484-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,8 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77484-76:
(7*7)+(6*7)+(5*4)+(4*8)+(3*4)+(2*7)+(1*6)=175
175 % 10 = 5
So 77484-76-5 is a valid CAS Registry Number.

77484-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-3,4-dibromopyrrolidine hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:77484-76-5 SDS

77484-76-5Relevant academic research and scientific papers

A New Approach to Allylamines and Pyrrolidines

Gajda, Tadeusz,Zwierzak, Andrzej

, p. 992 - 1002 (2007/10/02)

The 1,4-adducts 3a-c and 4, readily available from the reaction between diethyl N,N-dichlorophosphoramidate (1) and 1,3-dienes, were found to be convenient precursors for the efficient synthesis of the δ-chloroallylamine hydrochlorides 5a-d and N-phosphorylated allylamines 6a-c and 7.The three-step transformation of 3a-c affords the cis-3,4-dibromopyrrolidine hydrochlorides 10a-c.The preparation of the 2,5-dihydro-1H-pyrrole hydrochlorides 11a-c and trans-3,4-dibromopyrrolidine hydrochlorides 13a-c is also described.The stereochemistry of the reaction is studied.

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