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32941-30-3

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32941-30-3 Usage

General Description

1-(4-Pyridyl)heptan-1-one, also known as Pivampicillin, is a chemical compound with the molecular formula C12H15NO. It is a yellow, crystalline powder with a characteristic odor. Pivampicillin is commonly used as a precursor in the synthesis of various pharmaceuticals, particularly penicillin derivatives. It possesses antibacterial properties and is often used in the treatment of bacterial infections. Additionally, it has also been studied for its potential use as an anti-inflammatory agent. Pivampicillin is classified as a pyridine derivative and is important in the field of medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 32941-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,4 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32941-30:
(7*3)+(6*2)+(5*9)+(4*4)+(3*1)+(2*3)+(1*0)=103
103 % 10 = 3
So 32941-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-2-3-4-5-6-12(14)11-7-9-13-10-8-11/h7-10H,2-6H2,1H3

32941-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-pyridin-4-ylheptan-1-one

1.2 Other means of identification

Product number -
Other names 4-Heptanoylpyridine

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:32941-30-3 SDS

32941-30-3Downstream Products

32941-30-3Relevant articles and documents

Comparative inhibition of tetrameric carbonyl reductase activity in pig heart cytosol by alkyl 4-pyridyl ketones

Shimada, Hideaki,Tanigawa, Takahiro,Matayoshi, Kazunori,Katakura, Kazufumi,Babazono, Ken,Takayama, Hiroyuki,Murahashi, Tsuyoshi,Akita, Hiroyuki,Higuchi, Toshiyuki,Eto, Masashi,Imamura, Yorishige

, p. 397 - 400 (2014/06/09)

Context and objective: The present study is to elucidate the comparative inhibition of tetrameric carbonyl reductase (TCBR) activity by alkyl 4-pyridyl ketones, and to characterize its substrate-binding domain. Materials and methods: The inhibitory effect

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