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4,8-Decadien-1-ol, 4,8-dimethyl-10-(phenylsulfonyl)-, (E,E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

184763-00-6

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184763-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184763-00-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,7,6 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 184763-00:
(8*1)+(7*8)+(6*4)+(5*7)+(4*6)+(3*3)+(2*0)+(1*0)=156
156 % 10 = 6
So 184763-00-6 is a valid CAS Registry Number.

184763-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-(benzenesulfonyl)-4,8-dimethyldeca-4,8-dien-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:184763-00-6 SDS

184763-00-6Relevant academic research and scientific papers

Total synthesis of the proposed structure of astakolactin

Tonoi, Takayuki,Mameda, Keisuke,Fujishiro, Moe,Yoshinaga, Yutaka,Shiina, Isamu

, p. 2421 - 2427 (2014/12/12)

The first total synthesis of the proposed structure of astakolactin, a sesterterpene metabolite isolated from the marine sponge Cacospongia scalaris, has been achieved, mainly featuring Johnson-Claisen rearrangement, asymmetric Mukaiyama aldol reaction an

First asymmetric synthesis of the marine furanosesterterpene natural product, (18S)-variabilin, employing enzymatic desymmetrization of propanediol derivatives

Takabe, Kunihiko,Hashimoto, Hiroya,Sugimoto, Hideki,Nomoto, Masaru,Yoda, Hidemi

, p. 909 - 912 (2007/10/03)

An efficient and stereodefined process is described for the first preparation of the marine furanosesterterpene tetronic acid, (18S)-variabilin, featuring lipase-catalyzed asymmetric desymmetrization of two types of propanediol precursors incorporating the terpene skeleton.

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