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58851-77-7

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58851-77-7 Usage

Type

Diacetate derivative of 1a,2,7,7a-tetrahydronaphtho[2,3-b]oxirene-3,6-diyl

Physical State

White or light yellow solid

Usage

Commonly used in organic synthesis and chemical research

Structure

Oxacyclic structure

Application

Can be used as a building block in the preparation of various organic compounds

Safety

Potential hazards and toxicity; should be handled with care and used by trained professionals in a controlled laboratory setting

Safety Protocols

Proper safety protocols must be followed when handling this chemical

Check Digit Verification of cas no

The CAS Registry Mumber 58851-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,5 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58851-77:
(7*5)+(6*8)+(5*8)+(4*5)+(3*1)+(2*7)+(1*7)=167
167 % 10 = 7
So 58851-77-7 is a valid CAS Registry Number.

58851-77-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-acetyloxy-1a,2,7,7a-tetrahydronaphtho[6,7-b]oxiren-6-yl) acetate

1.2 Other means of identification

Product number -
Other names 6,7-epoxy-5,6,7,8-tetrahydro-1,4-diacetoxynaphthalene

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:58851-77-7 SDS

58851-77-7Relevant articles and documents

Synthesis of anthracyclinone precursor: 5,12-dihydroxy-1,3,4- trihydronaphthacene-2,6,11-quinone

Tririya, Gasirat,Zanger, Murray

, p. 3047 - 3059 (2007/10/03)

Two practical and efficient approaches for preparing large quantities of 5,12-dihydroxy-1,3,4-trihydronaphthacene-2,6,11-quinone 9 are described. Both synthetic approaches involve a simple route with a fewer number of steps and utilize readily available and inexpensive starting materials. Large-scale production of this precursor may prove to be useful for further research involving the synthesis of antineoplastic anthracyclines and development of their analogs with increased activity and decreased toxicity.

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