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62623-86-3

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62623-86-3 Usage

Chemical structure

A spiro compound with two hydroxyl groups located at the 11th and 12th positions.

Natural source

Commonly found in the essential oil of the vetiver plant, a tropical grass native to India.

Biological activities

Studied for potential antimicrobial, antioxidant, and anti-inflammatory properties.

Aroma compound

Identified as a key aroma compound in vetiver oil, contributing to its characteristic earthy, woody, and smoky scent.

Applications

Potential uses in the fragrance industry and pharmaceutical research due to its diverse biological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 62623-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,2 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62623-86:
(7*6)+(6*2)+(5*6)+(4*2)+(3*3)+(2*8)+(1*6)=123
123 % 10 = 3
So 62623-86-3 is a valid CAS Registry Number.

62623-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 11S,12-Dihydroxyspirovetiv-1(10)-en-2-one

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:62623-86-3 SDS

62623-86-3Upstream product

62623-86-3Downstream Products

62623-86-3Relevant articles and documents

Sesquiterpenoid spiro compounds from potato tubers infected with Phoma foveata and Fusarium spp.

Engstroem, Karin

, p. 985 - 990 (1998)

The main sesquiterpenoids found in potato tubers infected by the fungi Phoma foveata and Fusarium spp. were identified as the C-1' epimers of (2R,5S,10R)-2-(1',2'-dihydroxy-1'-methylethyl)-6,10-dimethyl-spiro[4,5]dec- 6-en-8-one and their 2'-O-β-D-glucopyranosides, by using NMR techniques, conformational analysis, CD measurements and chemical methods. The 1'S epimers predominated. The pattern of postinfectional metabolites in the stress zone and mycelia as well as in healthy tuber tissue was monitored by HPLC.

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