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3675-21-6

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3675-21-6 Usage

General Description

NSC3932, also known as 5-Methyl-2-phenyl-2-hexenal, is a chemical compound that is an aldehyde derivative. It is commonly used in the flavor and fragrance industry as a component in various products due to its sweet, citrus-like odor. In addition to its use in scents and flavorings, NSC3932 has also been studied for its potential anti-cancer and anti-inflammatory properties. Research suggests that it may have potential therapeutic applications in treating certain types of cancer and inflammatory conditions, although further studies are needed to fully understand its effects and mechanisms of action. As a result, NSC3932 continues to be of interest to the scientific and medical communities for its potential health benefits in addition to its use in commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3675-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3675-21:
(6*3)+(5*6)+(4*7)+(3*5)+(2*2)+(1*1)=96
96 % 10 = 6
So 3675-21-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2/c1-3-5(2)4-6(7)8/h4H,3H2,1-2H3,(H,7,8)/b5-4-

3675-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-methylpent-2-enoic acid

1.2 Other means of identification

Product number -
Other names RSFQOQOSOMBPEJ-PLNGDYQASA

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:3675-21-6 SDS

3675-21-6Relevant articles and documents

Carbonyl homologation via α-trimethylsilyl β-lactone rearrangements. A nonbasic alternative to the Wittig reaction

Black,Zhang,Huang,Smith,Yates

, p. 15 - 20 (2007/10/02)

Saturated and unsaturated aldehydes and ketones, when treated with trimethylsilylketene and BF3 for 16 hours, form β-lactones which spontaneously rearrange to α,β-unsaturated TMS esters; these hydrolyze during workup to form the corresponding carboxylic acids.

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