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N1-cyclohexyl-2-methylpropane-1,2-diamine is an organic compound with the molecular formula C11H23N. It is a derivative of propane-1,2-diamine, where one of the hydrogen atoms on the nitrogen atom is replaced by a cyclohexyl group, and the other hydrogen atom is replaced by a methyl group. N~1~-cyclohexyl-2-methylpropane-1,2-diamine is a colorless liquid with a molecular weight of 173.31 g/mol. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its amine functional groups, it can participate in various chemical reactions, such as alkylation, acylation, and condensation reactions, making it a versatile building block in organic synthesis.

1636-29-9

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1636-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1636-29-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1636-29:
(6*1)+(5*6)+(4*3)+(3*6)+(2*2)+(1*9)=79
79 % 10 = 9
So 1636-29-9 is a valid CAS Registry Number.

1636-29-9SDS

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 N<sup>1</sup>-Cyclohexyl-2-methyl-1,2-propanediamine

1.2 Other means of identification

Product number -
Other names N2-Cyclohexyl-1,1-dimethyl-aethandiyldiamin

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:1636-29-9 SDS

1636-29-9Relevant academic research and scientific papers

Synthesis of 1,2-diamines, 2-imidazolidinones and 2-imidazolidinethiones from α-haloimines

De Kimpe,D'Hondt

, p. 1013 - 1017 (2007/10/02)

α-Bromo- and α-chloroaldimines 1 are easily converted into α-azidoaldimines 2 which are reduced by lithium aluminum hydride to afford N-monoalkylated 1,2-diamines 3. In a similar way, aromatic α-bromoketimines 7 are transformed into the corresponding α-azidoketimines 8 and α-monoalkylated l,2-diamines 9. The 1,2-diamines, thus obtained, are converted into 2-imidazolidinones 4, 10 and 2-imidazolidinethiones 5, 11.

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