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3070-68-6

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3070-68-6 Usage

General Description

Methyl 2-methylidenehexanoate is a chemical compound that belongs to the ester group. It is a colorless liquid with a fruity odor, and is commonly used as a flavoring agent in the food and beverage industry. It is also used as a fragrance ingredient in perfumes and personal care products. Methyl 2-methylidenehexanoate is typically synthesized through the esterification of 2-methylidenehexanoic acid with methanol. It is important to handle this chemical with care as it can be harmful if ingested or inhaled, and it may cause irritation to the skin and eyes upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 3070-68-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3070-68:
(6*3)+(5*0)+(4*7)+(3*0)+(2*6)+(1*8)=66
66 % 10 = 6
So 3070-68-6 is a valid CAS Registry Number.

3070-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-methylidenehexanoate

1.2 Other means of identification

Product number -
Other names 2-methylenehexylcarbonic acid methyl ester

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:3070-68-6 SDS

3070-68-6Relevant articles and documents

A New Fragmentation Reaction of γ-Oxosulfonium Methylides

Watanabe, Yoshihiko,Takeda, Toyonori,Anbo, Keiji,Ueno, Yoshio,Toru, Takeshi

, p. 159 - 162 (2007/10/02)

Reactions of sulfonium methylides attached to a 5- or 6-membered cycloalkanone undergo the ring-fission as a major reaction course to give α-methylene-ω-(phenylthio)carboxylates, whereas sulfonium methylides attached to a larger ring give α-methylenecycloalkanones predominantly.Reactions of the acyclic compounds are also examined.

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