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2,2-dimethyl-1-phenylcyclopropylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109296-40-4

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109296-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109296-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,2,9 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 109296-40:
(8*1)+(7*0)+(6*9)+(5*2)+(4*9)+(3*6)+(2*4)+(1*0)=134
134 % 10 = 4
So 109296-40-4 is a valid CAS Registry Number.

109296-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-1-phenylcyclopropylamine

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:109296-40-4 SDS

109296-40-4Relevant academic research and scientific papers

A New Method for the Preparation of 2,2-Dialkylcyclopropylamines

Sulmon, Paul,Kimpe, Norbert De,Schamp, Niceas

, p. 1677 - 1678 (1986)

2,2-Dialkylcyclopropylamines have been prepared by a new synthetic method involving base-induced cyclization of β-chloroimines and subsequent hydrolysis.

Synthesis of 2,2-dialkylcyclopropylamines from β-chloroimines and application towards the synthesis of 1-amino-2,2-dialkylcyclopropane-carboxylic acids

De Kimpe,Sulmon,Boeykens

, p. 3389 - 3406 (2007/10/07)

Base-induced 1,5-dehydrochlorination of β-chloroimines, having a relatively acidic hydrogen atom at carbon-1 of the N-substituent (e.g. benzyl, methoxycarbonylmethyl, α-methylbenzyl), afforded N-cyclopropylimines which were easily hydrolyzed into cyclopropylamines. This synthetic methodology was applied to the synthesis of the potentially plant growth regulating 1-amino-2,2-dialkylcyclopropanecarboxylic acids via oxidation with catalytic ruthenium(IV)oxide/sodium periodate of suitably N-protected 1-aryl-2,2-dialkylcyclopropylamines.

SYNTHESIS OF 2,2-DIMETHYL-1-AMINOCYCLOPROPANECARBOXYLIC ACID FROM β-CHLOROIMINES

Kimpe, Norbert De,Sulmon, Paul,Schamp, Niceas

, p. 5029 - 5032 (2007/10/02)

2,2-Dimethyl-ACC, a potential plant growth regulator, was synthesized by cyclopropanation of β-chloroimines.

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