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NSC3932, also known as 5-Methyl-2-phenyl-2-hexenal, is a chemical compound that is an aldehyde derivative. It is recognized for its sweet, citrus-like odor and is commonly used in the flavor and fragrance industry. Beyond its commercial applications, NSC3932 has garnered attention for its potential anti-cancer and anti-inflammatory properties, making it a subject of interest for both scientific and medical research communities.

3675-21-6

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3675-21-6 Usage

Uses

Used in Flavor and Fragrance Industry:
NSC3932 is used as a flavoring agent and fragrance component for its distinctive sweet, citrus-like scent, enhancing the sensory experience of various products in this industry.
Used in Pharmaceutical Research:
NSC3932 is studied as a potential anti-cancer agent, with research indicating its possible therapeutic applications in treating certain types of cancer. Its mechanisms of action and effects are still under investigation, but the compound holds promise for future cancer treatments.
Used in Anti-Inflammatory Research:
NSC3932 is also being explored for its potential anti-inflammatory properties, suggesting that it may be beneficial in managing inflammatory conditions. Further studies are required to understand its full potential and efficacy in this area.

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 academic research and scientific papers

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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