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79296-92-7

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79296-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79296-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,9 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79296-92:
(7*7)+(6*9)+(5*2)+(4*9)+(3*6)+(2*9)+(1*2)=187
187 % 10 = 7
So 79296-92-7 is a valid CAS Registry Number.

79296-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(pyridin-3-ylmethyl)phosphanium,chloride

1.2 Other means of identification

Product number -
Other names pyridin-3-ylmethyltriphenylphosphonium chloride

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:79296-92-7 SDS

79296-92-7Relevant articles and documents

Br?nsted acid-catalysed conjugate addition of photochemically generated α-amino radicals to alkenylpyridines

Hepburn, Hamish B.,Melchiorre, Paolo

supporting information, p. 3520 - 3523 (2016/03/04)

The conjugate addition of α-amino radicals to alkenylpyridines has been accomplished by the synergistic merger of Br?nsted acid and visible light photoredox catalysis. Key to reaction development was the protonation of the alkenylpyridines that transientl

Phthalazine derivatives for treating inflammatory diseases

-

, (2008/06/13)

The invention relates to the treatment of an inflammatory disease, especially an inflammatory rheumatoid or rheumatic disease, and/or pain with an inhibitor of the activity of VEGF receptor tyrosine kinase of the formula I, wherein r is 0 to 2, n is 0 to

SYNTHESIS OF CAROTENOID ANALOGUES HAVING PYRIDINE, FURAN, AND TIOPHENE RINGS AS TERMINAL GROUPS

Brahmana, Hemat R.,Katsuyama, Kazuki,Inanaga, Junji,Katsuki, Tsutomi,Yamaguchi, Masaru

, p. 1695 - 1696 (2007/10/02)

Heteroaromatic carotenoid analogues having 2-pyridyl, 3-pyridyl, 2-furyl, 3-furyl, 2-thienyl, and 3-thienyl groups at both the ends of tetramethyloctadecanonaene chain, were synthesized and their spectral properties were examined.

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