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4996-15-0

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4996-15-0 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 80, p. 599, 1958 DOI: 10.1021/ja01536a021

Check Digit Verification of cas no

The CAS Registry Mumber 4996-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4996-15:
(6*4)+(5*9)+(4*9)+(3*6)+(2*1)+(1*5)=130
130 % 10 = 0
So 4996-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H5NO4/c11-9(12)5-4-7-2-1-3-8(6-7)10(13)14/h1-3,6H,(H,11,12)

4996-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-nitrophenyl)prop-2-ynoic acid

1.2 Other means of identification

Product number -
Other names 3-Nitro-phenyl-acetylencarbonsaeure

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:4996-15-0 SDS

4996-15-0Relevant articles and documents

Oxidant- and additive-free simple synthesis of 1,1,2-triiodostyrenes by one-pot decaroboxylative iodination of propiolic acids

Ghosh, Subhankar,Ghosh, Rajat,Chattopadhyay, Shital K.

supporting information, (2020/09/15)

A metal- and oxidant-free facile synthesis of a range of 1,1,2-triiodostryrene derivatives has been developed which utilizes a simple decarboxylative triiodination of propiolic acids using molecular iodine and sodium acetate in a one-pot manner. Electron-

Protonation of 3-arylpropynoic acid derivatives in superacids

Walspurger,Vasil'ev,Sommer,Pale,Savechenkov,Rudenko

, p. 1485 - 1492 (2007/10/03)

According to the 1H and 13C NMR data, 3-arylpropynoic acids and their esters XC6Hn-C≡C-CO2R (R = H, Me, Et) having electron-withdrawing substituents in the benzene ring (X = NO2, CN, COMe,

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