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3742-63-0

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  • Acetic acid,2-(1-methylethylidene)hydrazide

    Cas No: 3742-63-0

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3742-63-0 Usage

General Description

Acetic acid isopropylidene-hydrazide, also known as AIIH, is a chemical compound derived from acetic acid and hydrazine. It is commonly used as a corrosion inhibitor and is also used in the production of pharmaceuticals and agrochemicals. AIIH is a colorless liquid with a faint odor, and it is soluble in water and alcohol. It is known for its ability to form complexes with metal ions, making it useful in chemical processes and industrial applications. Additionally, AIIH is known for its antimicrobial properties, making it ideal for use in disinfectants and antibacterial products. Overall, AIIH is a versatile compound with a wide range of industrial and scientific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3742-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,4 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3742-63:
(6*3)+(5*7)+(4*4)+(3*2)+(2*6)+(1*3)=90
90 % 10 = 0
So 3742-63-0 is a valid CAS Registry Number.

3742-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(propan-2-ylideneamino)acetamide

1.2 Other means of identification

Product number -
Other names N'-(1-methylethylidene)acetohydrazide

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:3742-63-0 SDS

3742-63-0Relevant articles and documents

Reaction of 2-acetyl-5-methyl-2H-1,2,3-diazaphosphole with butane-2,3-diol

Khusainova, Narkis G.,Mostovaya, Olga A.,Azancheev, Nail M.,Litvinov, Igor A.,Krivolapov, Dmitry B.,Cherkasov, Rafael A.

, p. 212 - 214 (2004)

The reaction of 2-acetyl-5-methyl-2H-1,2,3-diazaphosphole with (rac)-butane-2,3-diol at temperatures below 0 °C leads to the formation of a hydrospirophosphorane containing both a diazaphospholene and a dioxaphospholane ring system and a β-hydroxy-alkoxy-1,2,3-diazaphospholene. On heating, these products form a hydrospirotetraoxaphosphorane, its tautomeric monocyclic β-hydroxyalkylphosphite and N-acetyl-N'-isopropylidene-hydrazine.

Catalytic hydrophosphorylation of alkyl- and acylhydrazones

Matveeva,Podrugina,Kolesnikova,Prisyazhnoi,Karateev,Zefirov

experimental part, p. 418 - 424 (2011/02/17)

N-Boc- and N-acylhydrazino phosphonates were obtained for the first time by hydrophos- phorylation of the appropriate hydrazones of aliphatic and aromatic aldehydes and heterocyclic and aliphatic ketones in the presence of [tetra(tert-butyl)phthalocyanine

1-Acyl-2-alkylhydrazines by the Reduction of Acylhydrazones

Pei-Lin-Wu,Peng, Shao-Yu,Magrath, Joe

, p. 435 - 438 (2007/10/02)

1-Acyl-2-alkylhydrazines were easily prepared by the reduction of acylhydrazones with triethylsilane in the presence of trifluoroacetic acid.

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