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Isosclareol, a naturally occurring sesquiterpene alcohol, is a chemical compound found in various plants, particularly in the genus Artemisia. It is known for its potential anti-inflammatory, antimicrobial, and anticancer properties, making it a subject of interest in pharmaceutical research. Isosclareol is also used in the synthesis of other bioactive compounds and has been studied for its potential role in treating various diseases and conditions. Its structure and biological activities are of significant importance in the field of natural product chemistry and drug development.

4630-08-4

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4630-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4630-08-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,3 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4630-08:
(6*4)+(5*6)+(4*3)+(3*0)+(2*0)+(1*8)=74
74 % 10 = 4
So 4630-08-4 is a valid CAS Registry Number.

4630-08-4SDS

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 (1R,2R,4aS,8aS)-1-(3-hydroxy-3-methylpent-4-enyl)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol

1.2 Other means of identification

Product number -
Other names (13S)-Labd-14-ene-8,13-diol

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:4630-08-4 SDS

4630-08-4Relevant academic research and scientific papers

A SHORT SYNTHESIS OF AMBROX FROM SCLAREOL

Decorzant, Rene,Vial, Christian,Naf, Ferdinand,Whitesides, George M.

, p. 1871 - 1880 (2007/10/02)

A two-step transformation of sclareol into Ambrox (overall yield 11-12percent) via β-cleavage of an alkoxy radical intermediate is described.

STRUCTURE OF NEW BROMODITERPENES, PINNATOLS, FROM THE MARINE RED ALGA LAURENCIA PINNATA YAMADA

Fukuzawa, Akio,Miyamoto, Mitsuaki,Kumagai, Yoshikazu,Abiko, Atsushi,Takaya, Yoshiaki,Masamune, Tadashi

, p. 1259 - 1262 (2007/10/02)

The structure of new bromoditerpenes named pinnatols A, B, C, and D, isolated from the title alga, was determined on the basis of the chemical and spectral data.

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