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47192-97-2

47192-97-2

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47192-97-2 Usage

Chemical Properties

Pale Yellow Solid

Check Digit Verification of cas no

The CAS Registry Mumber 47192-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,1,9 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 47192-97:
(7*4)+(6*7)+(5*1)+(4*9)+(3*2)+(2*9)+(1*7)=142
142 % 10 = 2
So 47192-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H16O4/c1-11(19)22-18-16(21-3)9-7-13-5-4-12-6-8-14(20-2)10-15(12)17(13)18/h4-10H,1-3H3

47192-97-2SDS

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 (3,6-dimethoxyphenanthren-4-yl) acetate

1.2 Other means of identification

Product number -
Other names 3,6-Dimethoxy-4-acetoxyphenanthrene

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:47192-97-2 SDS

47192-97-2Downstream Products

47192-97-2Relevant articles and documents

Thebaine Rearrangements: Nonclassical D Ring Migrations

Allen, Andrew C.,Cooper, Donald A.,Moore, James M.,Teer, Charles B.

, p. 3462 - 3465 (2007/10/02)

3,6-Dimethoxy-4-acetoxy-5-phenanthrene (3) and its isomer 3,6-dimethoxy-4-acetoxy-8-phenanthrene (4) have been detected as manufacturing byproducts at trace levels in illicit heroin.These compounds are novel rearrangement products obtained by the action of acetic anhydride (Ac2O) on thebaine (1).The syntheses of 3 and 4 from 1 proceed via the intermediate Δ5,7,9(14)-N-acetyldesthebaine (2).Structural characterization and optimization of synthetic conditions for 3 and 4 are described.A brief discussion is also giving concerning other neutral products of 1 obtained under Ac2O conditions.

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