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40438-64-0

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40438-64-0 Usage

Uses

Different sources of media describe the Uses of 40438-64-0 differently. You can refer to the following data:
1. Catalyst for cycloaddition reactions in the presence of rhodium-catalysts.
2. Catalyst for cycloaddition reactions in the presence of rhodium-catalysts

Check Digit Verification of cas no

The CAS Registry Mumber 40438-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,3 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40438-64:
(7*4)+(6*0)+(5*4)+(4*3)+(3*8)+(2*6)+(1*4)=100
100 % 10 = 0
So 40438-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H32NP/c1-21(2)17-13-15-20(16-14-17)22(18-9-5-3-6-10-18)19-11-7-4-8-12-19/h13-16,18-19H,3-12H2,1-2H3

40438-64-0SDS

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 4-dicyclohexylphosphanyl-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names 4-(Dicyclohexylphosphino)-N,N-dimethylaniline

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:40438-64-0 SDS

40438-64-0Upstream product

40438-64-0Relevant articles and documents

Method for synthesizing [4-(N,N-dimethylamino)phenyl]dialkylphosphine

-

Paragraph 0010; 0011, (2017/10/31)

The invention discloses a method for synthesizing [4-(N,N-dimethylamino)phenyl]dialkylphosphine and belongs to the field of organic synthesis. According to the method, N,N-dimethylaniline as a raw material and 4-dimethylamino-pyridine as a base are reacted, in water-free oxygen-free atmosphere, with dialkyl phosphorous chloride under the catalytic action of cuprous acetate to generate [4-(N,N-dimethylamino)phenyl]dialkylphosphine. Compared with the prior art, the method has the advantages that reaction conditions are mild, operating is simple, the yield is high, the materials are simple and easy to obtain, production cost is reduced and the method is suitable for industrial production.

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