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63113-01-9

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63113-01-9 Usage

General Description

3-hydroxy-7-methyl-2-benzofuran-1(3H)-one, also known as alpha-cedrene, is a chemical compound found in the essential oil of cedarwood. It is a colorless to pale yellow liquid with a sweet and woody odor. Alpha-cedrene is commonly used in the fragrance industry as a fixative and as a scent additive in perfumes, colognes, and other personal care products. It is also used as a flavoring agent in the food industry. In addition to its aromatic properties, alpha-cedrene has been studied for its potential medicinal properties, including anti-inflammatory, antioxidant, and anti-cancer effects.

Check Digit Verification of cas no

The CAS Registry Mumber 63113-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,1 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63113-01:
(7*6)+(6*3)+(5*1)+(4*1)+(3*3)+(2*0)+(1*1)=79
79 % 10 = 9
So 63113-01-9 is a valid CAS Registry Number.

63113-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-3-hydroxy-7-methyl-3H-2-benzofuran-1-one

1.2 Other means of identification

Product number -
Other names 7-Methylphthalaldehydsaeure

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:63113-01-9 SDS

63113-01-9Relevant articles and documents

Chiral Bicyclic Imidazole-Catalyzed Acylative Dynamic Kinetic Resolution for the Synthesis of Chiral Phthalidyl Esters

Zhou, Muxing,Gridneva, Tatiana,Zhang, Zhenfeng,He, Ende,Liu, Yangang,Zhang, Wanbin

, p. 1641 - 1645 (2020/11/30)

Utilizing a chiral bicyclic imidazole organocatalyst and adopting a continuous injection process, an alternative route has been developed for the efficient synthesis of chiral phthalidyl ester prodrugs via dynamic kinetic resolution of 3-hydroxyphthalides through enantioselective acylation (up to 99 % ee). The computational studies suggest a general base catalytic mechanism differing from the widely accepted nucleophilic catalytic mechanism. The structure analysis of the key transition states shows that the CH-π interactions and not the previously considered cation/π-π interactions between the catalyst and substrate is the dominant factor giving rise to the observed stereocontrol.

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