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16642-52-7

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16642-52-7 Usage

General Description

2,2-Dimethyl-3-pentenoic acid is a chemical compound with the molecular formula C7H12O2. It is also known as isoamyl vinyl ketone and is classified as an alpha, beta-unsaturated ketone. 2,2-Dimethyl-3-pentenoic acid is a colorless liquid with a fruity odor and is commonly used as a flavoring agent in the food industry. Additionally, it is also used as an intermediate in the synthesis of organic compounds and pharmaceuticals. 2,2-Dimethyl-3-pentenoic acid has potential health hazards and should be handled with care, as it is an irritant to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 16642-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,4 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16642-52:
(7*1)+(6*6)+(5*6)+(4*4)+(3*2)+(2*5)+(1*2)=107
107 % 10 = 7
So 16642-52-7 is a valid CAS Registry Number.

16642-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethylpent-3-enoic acid

1.2 Other means of identification

Product number -
Other names 2,2-Dimethyl-3-pentenoic acid

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:16642-52-7 SDS

16642-52-7Downstream Products

16642-52-7Relevant articles and documents

Divergent Reactivity of α,α-Disubstituted Alkenyl Hydrazones: Bench Stable Cyclopropylcarbinyl Equivalents

Ritchie, Nina F. C.,Zahara, Adam J.,Wilkerson-Hill, Sidney M.

, p. 2101 - 2106 (2022/02/14)

Herein we report the divergent reactivity of 2,2-dialkyl-3-(E)-alkenyl N-tosylhydrazones using Pd-catalyzed cross-coupling conditions, which enable the Z-selective synthesis of 3-aryl-1,4-dienes and gem-dialkyl vinylcyclopropanes. We found that the dialky

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