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1,4-Benzodioxin-2-methanol, 2,3-dihydro-6-methyl- is a chemical compound with the molecular formula C9H10O3. It is a derivative of benzodioxin, featuring a methanol group at the 2-position and a methyl group at the 6-position. 1,4-Benzodioxin-2-methanol, 2,3-dihydro-6-methyl- is characterized by its dihydro structure, which means it has two hydrogen atoms added to the benzene ring, resulting in a saturated six-membered ring. It is an organic compound with potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

3635-13-0

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3635-13-0 Usage

Molecular weight

180.2 g/mol

Appearance

Colorless or slightly yellow liquid

Odor

Pleasant

Natural occurrence

Found in plants like sassafras, basil, and nutmeg

Uses

a. Synthesis of fragrances
b. Synthesis of flavors
c. Synthesis of insecticides
d. Precursor in the manufacture of MDMA (ecstasy)

Health concerns

Potential carcinogenic and hepatotoxic effects

Regulatory status

Controlled substance in many countries with restricted use

Check Digit Verification of cas no

The CAS Registry Mumber 3635-13-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,3 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3635-13:
(6*3)+(5*6)+(4*3)+(3*5)+(2*1)+(1*3)=80
80 % 10 = 0
So 3635-13-0 is a valid CAS Registry Number.

3635-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-Methyl-2,3-dihydro-1,4-benzodioxin-2-yl)methanol

1.2 Other means of identification

Product number -
Other names 2-Hydroxymethyl-6-methyl-1,4-benzodioxane

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:3635-13-0 SDS

3635-13-0Downstream Products

3635-13-0Relevant academic research and scientific papers

Study of the O-glycidylation of natural phenolic compounds. the relationship between the phenolic structure and the reaction mechanism

Aouf, Chahinez,Le Guernevé, Christine,Caillol, Sylvain,Fulcrand, Hélène

, p. 1345 - 1353 (2013/02/23)

The O-alkylation reaction by epichlorohydrin of some natural phenolic compounds such as 4-methylcatechol, gallic acid, protocatechuic acid, pyrogallol and resorcinol was investigated. Phenolic compounds reacted first with epichlorohydrin in the presence of benzyltriethylammonium chloride as phase transfer catalyst. Then, an aqueous solution of sodium hydroxide was added. It was demonstrated that the two competitive mechanisms involved in the O-alkylation reaction were highly dependent of the starting material. The O-alkylated products obtained in this reaction could be further used as bisphenol A substitutes in the synthesis of epoxy resins pre-polymers.

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