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FORMAMIDOXIME is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

624-82-8

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624-82-8 Usage

Uses

Formamidoxime may be used as inhibitor of DNA synthesis.

Biochem/physiol Actions

Formamidoxime undergoes oxidative cleavage of C==N bonds in tracheal smooth muscle cells catalyzed by liver cytochrome P450 producing NO. It inhibits replicative DNA synthesis. It has antitumor activity against L1210 leukemia.

Check Digit Verification of cas no

The CAS Registry Mumber 624-82-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 624-82:
(5*6)+(4*2)+(3*4)+(2*8)+(1*2)=68
68 % 10 = 8
So 624-82-8 is a valid CAS Registry Number.
InChI:InChI=1/CH4N2O/c2-1-3-4/h1,4H,(H2,2,3)

624-82-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • Aldrich

  • (140198)  Formamidoxime  99%

  • 624-82-8

  • 140198-5G

  • 2,261.61CNY

  • Detail

  • Aldrich

  • (140198)  Formamidoxime  99%

  • 624-82-8

  • 140198-25G

  • 7,605.00CNY

  • Detail

624-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name FORMAMIDOXIME

1.2 Other means of identification

Product number -
Other names Methanimidamide, N-hydroxy-

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:624-82-8 SDS

624-82-8Relevant academic research and scientific papers

Survey Reactivity of Some Substituted Quinazolinones with Pentafluoro(chloro)pyridine

Ranjbar-Karimi, Reza,Davodian, Tayebeh,Mehrabi, Hossein

, p. 475 - 480 (2017/12/28)

A new series of 4-hetroaryl substituted quinazolines were designed and synthesized by the reaction of pentafluoro(chloro)pyridine and 2-substituted quinazolinone. The aromatic nucleophilic substitution of pentafluoro(chloro)pyridine with quinazolinone occurs at the 4-position of pyridine ring by the oxygen site (O-centered nucleophile) of quinazolinone. The structures of all the compounds were confirmed by IR, 1H NMR, 19F NMR, and 13C NMR spectroscopy as well as elemental analysis.

Novel process for the preparation of pyrazolopyrimidinones

-

, (2008/06/13)

There is provided a process for the production a compound of general formula I: wherein A, R1, R2, R3 and R4 have meanings given in the description, which process comprises the reaction of a compound of formula II, wherein Rx is a group substitutable by an aminopyrazole, with a compound of general formula III

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