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76177-02-1

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76177-02-1 Usage

Description

(1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol is a chemical compound with a molecular formula C13H14O2. It is an alcohol derivative of acenaphthene, a polycyclic aromatic hydrocarbon. (1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol has two stereocenters, resulting in four possible stereoisomers. It is a white to off-white solid, with a molecular weight of 202.25 g/mol. (1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol has potential applications in organic synthesis and as a building block for the preparation of biologically active compounds. Its exact uses and properties may vary depending on its specific stereoisomeric configuration and synthetic preparation.

Uses

Used in Organic Synthesis:
(1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure and functional groups make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
(1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol is used as a precursor for the preparation of biologically active compounds. Its stereochemistry and chemical properties can be leveraged to develop new drugs with specific therapeutic effects. (1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol's potential as a building block allows for the exploration of novel drug candidates with improved efficacy and selectivity.
Used in Agrochemical Industry:
(1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol is used as a starting material for the development of agrochemicals, such as pesticides and herbicides. Its structural features can be utilized to create new molecules with enhanced activity against pests and weeds, contributing to more effective and sustainable agricultural practices.
Used in Specialty Chemicals:
(1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol is used as a key component in the production of specialty chemicals, which have applications in various industries such as coatings, adhesives, and materials science. Its unique properties can be exploited to develop innovative products with improved performance characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 76177-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,7 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76177-02:
(7*7)+(6*6)+(5*1)+(4*7)+(3*7)+(2*0)+(1*2)=141
141 % 10 = 1
So 76177-02-1 is a valid CAS Registry Number.

76177-02-1SDS

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 (1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol

1.2 Other means of identification

Product number -
Other names -

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:76177-02-1 SDS

76177-02-1Relevant articles and documents

1,2-DERIVATIVES OF ACENAPHTHYLENE. II. THERMAL STABILITY OF ACENAPHTHYLENE OXIDE AND ITS REACTION WITH ALCOHOLS

Anikin, V. F.,Levandovskaya, T. I.

, p. 1762 - 1766 (2007/10/02)

Acenaphthylene oxide can be obtained with a high yield from acenaphthylene chlorohydrin acetate.When heated above 130 deg C, it isomerizes to acenaphthenone.With alcohols and potassium hydroxide it is converted into E-1,2-dihydro-1-alkoxy-2-hydroxy derivatives of acenaphthylene.

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