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Decanoic acid, triphenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78950-72-8

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78950-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78950-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,5 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78950-72:
(7*7)+(6*8)+(5*9)+(4*5)+(3*0)+(2*7)+(1*2)=178
178 % 10 = 8
So 78950-72-8 is a valid CAS Registry Number.

78950-72-8SDS

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 triphenylmethyl decanoate

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:78950-72-8 SDS

78950-72-8Downstream Products

78950-72-8Relevant academic research and scientific papers

EASY PREPARATION OF TRIPHENYLMETHYL CARBOXYLATES.

Hashimoto,Hayashi,Noyori

, p. 1431 - 1432 (2007/10/02)

A new method for triphenylmethylation of carboxylic acids and phenol is disclosed.

A FACILE PROCEDURE FOR O-TRITYLATION

Murata, S.,Noyori, R.

, p. 2107 - 2108 (2007/10/02)

The title operation is achieved via readily accessible organosilicon compounds.

TRIMETHYLSILYL TRIFLATE IN ORGANIC SYNTHESIS

Noyori, R.,Murata, S.,Suzuki, M.

, p. 3899 - 3910 (2007/10/02)

Trimethylsilyl triflate is a powerful silylating agent for organic compounds and acts as a catalyst which accelerates a variety of nucleophilic reactions in aprotic media.The reactions proceed via one-center, electrophilic coordination of the silyl group to hetero functional groups and exhibit unique selectivities.

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