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100538-95-2

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100538-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100538-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,3 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100538-95:
(8*1)+(7*0)+(6*0)+(5*5)+(4*3)+(3*8)+(2*9)+(1*5)=92
92 % 10 = 2
So 100538-95-2 is a valid CAS Registry Number.

100538-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexylmethyl-cyclopentylmethyl-amine

1.2 Other means of identification

Product number -
Other names Cyclohexylmethyl-cyclopentylmethyl-amine

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:100538-95-2 SDS

100538-95-2Relevant articles and documents

Anti-Markovnikov Hydroamination of Unactivated Alkenes with Primary Alkyl Amines

Miller, David C.,Ganley, Jacob M.,Musacchio, Andrew J.,Sherwood, Trevor C.,Ewing, William R.,Knowles, Robert R.

supporting information, p. 16590 - 16594 (2019/11/03)

We report here a photocatalytic method for the intermolecular anti-Markovnikov hydroamination of unactivated olefins with primary alkyl amines to selectively furnish secondary amine products. These reactions proceed through aminium radical cation (ARC) intermediates and occur at room temperature under visible light irradiation in the presence of an iridium photocatalyst and an aryl thiol hydrogen atom donor. Despite the presence of excess olefin, high selectivities are observed for secondary over tertiary amine products, even though the secondary amines are established substrates for ARC-based olefin amination under similar conditions.

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