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65974-17-6

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65974-17-6 Usage

General Description

2-Methyl-[1,4]diazepane, also known as 1,4-Diazepane-2-methanol, is a chemical compound with the formula C7H16N2O. It belongs to the class of organic molecules known as diazepanes and is used in the synthesis of pharmaceuticals and other organic compounds. It is a colorless liquid with a faint odor and is soluble in water and organic solvents. There is limited information available about its specific uses and potential hazards, so care should be taken when handling this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 65974-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,7 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65974-17:
(7*6)+(6*5)+(5*9)+(4*7)+(3*4)+(2*1)+(1*7)=166
166 % 10 = 6
So 65974-17-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2/c1-6-5-7-3-2-4-8-6/h6-8H,2-5H2,1H3

65974-17-6SDS

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 2-methyl-1,4-diazepane

1.2 Other means of identification

Product number -
Other names 2-Methyl-hexahydro-[1,4]diazepin

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:65974-17-6 SDS

65974-17-6Relevant articles and documents

Biocatalytic Access to Piperazines from Diamines and Dicarbonyls

Borlinghaus, Niels,Gergel, Sebastian,Nestl, Bettina M.

, p. 3727 - 3732 (2018/04/14)

Given the widespread importance of piperazines as building blocks for the production of pharmaceuticals, an efficient and selective synthesis is highly desirable. Here we show the direct synthesis of piperazines from 1,2-dicarbonyl and 1,2-diamine substrates using the R-selective imine reductase from Myxococcus stipitatus as biocatalyst. Various N- and C-substituted piperazines with high activity and excellent enantioselectivity were obtained under mild reaction conditions reaching up to 8.1 g per liter.

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