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2-Methylpropanal semicarbazone is a chemical compound derived from 2-methylpropanal, also known as isobutyraldehyde, and semicarbazide. It is formed through a condensation reaction between the aldehyde group of 2-methylpropanal and the semicarbazide molecule. This reaction results in the formation of a semicarbazone derivative, which is a type of Schiff base. 2-Methylpropanal semicarbazone is an organic compound with the molecular formula C6H13N2O2 and is used in various applications, including as an analytical reagent for the detection and determination of aldehydes and ketones. It is also employed in the synthesis of other organic compounds and pharmaceuticals. The compound is characterized by its ability to form colored complexes with metal ions, which can be useful in analytical chemistry for the identification and quantification of these ions.

592-64-3

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592-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 592-64-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 592-64:
(5*5)+(4*9)+(3*2)+(2*6)+(1*4)=83
83 % 10 = 3
So 592-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H11N3O/c1-4(2)3-7-8-5(6)9/h3-4H,1-2H3,(H3,6,8,9)

592-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-2-methylpropylideneamino]urea

1.2 Other means of identification

Product number -
Other names Isobutyraldehyde,semicarbazone

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:592-64-3 SDS

592-64-3Relevant academic research and scientific papers

Synthesis of 2-amino-1,3,4-oxadiazoles and 2-Amino-1,3,4-thiadiazoles via sequential condensation and I2-mediated oxidative C-O/C-S bond formation

Niu, Pengfei,Kang, Jinfeng,Tian, Xianhai,Song, Lina,Liu, Hongxu,Wu, Jie,Yu, Wenquan,Chang, Junbiao

, p. 1018 - 1024 (2015/01/30)

2-Amino-substituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles were synthesized via condensation of semicarbazide/thiosemicarbazide and the corresponding aldehydes followed by I2-mediated oxidative C-O/C-S bond formation. This transition-metal-free sequential synthesis process is compatible with aromatic, aliphatic, and cinnamic aldehydes, providing facile access to a variety of diazole derivatives bearing a 2-amino substituent in an efficient and scalable fashion.

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