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1H-Pyrrolizine-7-carboxamide, 2,3,5,6-tetrahydro-1-methyl-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106032-26-2

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106032-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106032-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,3 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106032-26:
(8*1)+(7*0)+(6*6)+(5*0)+(4*3)+(3*2)+(2*2)+(1*6)=72
72 % 10 = 2
So 106032-26-2 is a valid CAS Registry Number.

106032-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,6-tetrahydro-1-methyl-7-(N-phenyl)carbamoyl-1H-pyrrolizine

1.2 Other means of identification

Product number -
Other names 7-Methyl-2,5,6,7-tetrahydro-3H-pyrrolizine-1-carboxylic acid phenylamide

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:106032-26-2 SDS

106032-26-2Relevant academic research and scientific papers

Ring transformation of 1,2,3,5,6,7-hexahydropyrrolizinium perchlorates into 1-substituted 5-oxoperhydroazocines

Sumoto,Mibu,Irie,Abe,Miyano

, p. 577 - 580 (2007/10/02)

A facile ring transformation of 1,2,3,5,6,7-hexahydropyrrolizinium perchlorates (1 and 2) to 1-substituted 5-oxoperhydroazocines (5) is described. The spectroscopic and chemical properties of these products are also presented.

A NEW ROUTE TO 1-ACYL-5-OXOPERHYDROAZOCINE CORE USING 1,2,3,5,6,7-HEXAHYDROPYRROLIZINIUM PERCHLORATES

Miyano, Seiji,Mibu, Nobuko,Irie, Michiko,Sumoto, Kunihiro

, p. 2121 - 2126 (2007/10/02)

A convenient simple method for the synthesis of 1-substituted 5-oxoperhydroazocinea (1) is described.The method consists of N-acylation of 5-oxoperhydroazocine which is one of the tautomers of the pseudobase (3) generated by the treatment of 1,2,3,5,6,7-hexahydropyrrolizinium perchlorate with aqueous alkali.

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