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AKOS BAR-2295 is a chemical compound primarily used as a catalyst in various industrial processes. It is a member of the boron-based catalysts family, specifically a boron trifluoride etherate, and is known for its effectiveness in promoting the formation of carbon-carbon bonds. This catalyst is particularly useful in the synthesis of various organic compounds, such as alkenes and alkynes, through reactions like hydroboration and Suzuki-Miyaura coupling. Its stability and reactivity make it a valuable tool in the field of organic chemistry, contributing to the production of pharmaceuticals, agrochemicals, and other specialty chemicals.

5002-01-7

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5002-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5002-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5002-01:
(6*5)+(5*0)+(4*0)+(3*2)+(2*0)+(1*1)=37
37 % 10 = 7
So 5002-01-7 is a valid CAS Registry Number.

5002-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(2-methylphenyl)phenyl]acetic acid

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:5002-01-7 SDS

5002-01-7Upstream product

5002-01-7Downstream Products

5002-01-7Relevant academic research and scientific papers

Photostimulated reactions of phenylacetic acid dianions with aryl halides. Influence of the metallic cation on the regiochemistry of arylation.

Nwokogu,Wong,Greenwood,Wolfe

, p. 2643 - 2646 (2007/10/03)

[reaction: see text]Phenylacetic acid dianions react via what appears to be an S(RN)1 process with aryl halides under photostimulation to afford aryl substitution products 5 and 6. When the counterion is K+, only 4-biphenylacetic acids 5 are obtained. Both alpha- and para-coupling occurs with Na+ to give a mixture of 5 and 6, while exclusive formation of diphenylacetic acids 6 is observed with the dilithio salt of 1.

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