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40885-82-3

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40885-82-3 Usage

General Description

2-(Phenylhydrazono)malonic acid is a chemical compound that is a derivative of malonic acid. It features a phenylhydrazine group, which consists of a phenyl ring attached to a hydrazine functional group. The compound is used in organic synthesis as a reagent for the preparation of various organic compounds. It has potential applications in the pharmaceutical and agrochemical industries, as well as in the production of dyes and pigments. Additionally, it has been studied for its potential biological activities, including antibacterial and antifungal properties. Overall, 2-(phenylhydrazono)malonic acid is a versatile chemical with various potential applications in the field of organic chemistry and beyond.

Check Digit Verification of cas no

The CAS Registry Mumber 40885-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,8 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40885-82:
(7*4)+(6*0)+(5*8)+(4*8)+(3*5)+(2*8)+(1*2)=133
133 % 10 = 3
So 40885-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O4/c12-8(13)7(9(14)15)11-10-6-4-2-1-3-5-6/h1-5,10H,(H,12,13)(H,14,15)

40885-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(phenylhydrazinylidene)propanedioic acid

1.2 Other means of identification

Product number -
Other names Mesoxalsaeure-phenylhydrazon

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:40885-82-3 SDS

40885-82-3Relevant articles and documents

Distinct CCK-2 receptor conformations associated with β-arrestin-2 recruitment or phospholipase-C activation revealed by a biased antagonist

Magnan, Rémi,Escrieut, Chantal,Gigoux, Véronique,De, Kavita,Clerc, Pascal,Niu, Fan,Azema, Joelle,Masri, Bernard,Cordomi, Arnau,Baltas, Michel,Tikhonova, Irina G.,Fourmy, Daniel

supporting information, p. 2560 - 2573 (2013/03/29)

Seven-transmembrane receptors (7TMRs), also termed G protein-coupled receptors (GPCRs), form the largest class of cell surface membrane receptors, involving several hundred members in the human genome. Nearly 30% of marketed pharmacological agents target

Novel benzodiazepine photoaffinity probe stereoselectively labels a site deep within the membrane-spanning domain of the cholecystokinin receptor

Hadac, Elizabeth M.,Dawson, Eric S.,Darrow, James W.,Sugg, Elizabeth E.,Lybrand, Terry P.,Miller, Laurence J.

, p. 850 - 863 (2007/10/03)

An understanding of the molecular basis of drug action provides opportunities for refinement of drug properties and for development of more potent and selective molecules that act at the same biological target. In this work, we have identified the active

Solid phase synthesis of 6-acylamino-1-alkyl/aryl-4-oxo-1,4- dihydrocinnoline-3-carboxamides

Sereni, Laura,Tató, Marco,Sola, Francesco,Brill, Wolfgang K.-D.

, p. 8561 - 8577 (2007/10/03)

6-Acylmino-1-alkyl/aryl-4-oxo-1,4-dihydrocinnoline-3-carboxamides were synthesized in parallel from 6-nitro-4-oxo-1,4-dihydrocinnoline-3-carboxylic acid. The latter formed amides with amines bound to polystyrene-based resins via acid-labile linkers. N1 an

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