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1'-acetoxysafrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34627-78-6

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34627-78-6 Usage

Chemical Class

Allylbenzenes

Derivative of

Safrole

Natural Occurrence

Found in sassafras oil

Common Use

Synthesis of complex organic compounds

Application

Production of pharmaceuticals and perfumes

Illicit Use

Precursor chemical in the synthesis of MDMA (ecstasy)

Legal Status

Controlled substance in many countries

Regulation

Strictly regulated production, distribution, and use

Check Digit Verification of cas no

The CAS Registry Mumber 34627-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,2 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34627-78:
(7*3)+(6*4)+(5*6)+(4*2)+(3*7)+(2*7)+(1*8)=126
126 % 10 = 6
So 34627-78-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O4/c1-3-10(16-8(2)13)9-4-5-11-12(6-9)15-7-14-11/h3-6,10H,1,7H2,2H3

34627-78-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,3-benzodioxol-5-yl)prop-2-enyl acetate

1.2 Other means of identification

Product number -
Other names 1'-Acetoxysafrole

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:34627-78-6 SDS

34627-78-6Downstream Products

34627-78-6Relevant articles and documents

Hydroxymethylation beyond Carbonylation: Enantioselective Iridium-Catalyzed Reductive Coupling of Formaldehyde with Allylic Acetates via Enantiotopic π-Facial Discrimination

Garza, Victoria J.,Krische, Michael J.

supporting information, p. 3655 - 3658 (2016/04/09)

Chiral iridium complexes modified by SEGPHOS catalyze the 2-propanol-mediated reductive coupling of branched allylic acetates 1a-1o with formaldehyde to form primary homoallylic alcohols 2a-2o with excellent control of regio- and enantioselectivity. These

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