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2,6-Nonadien-1-ol, 3,7-dimethyl-9-(phenylsulfonyl)-8-[(tetrahydro-2H-pyran-2-yl)oxy]-9-(2,6, 6-trimethyl-1-cyclohexen-1-yl)-, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103905-07-3

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  • 2,6-Nonadien-1-ol, 3,7-dimethyl-9-(phenylsulfonyl)-8-[(tetrahydro-2H-pyran-2-yl)oxy]-9-(2,6, 6-trimethyl-1-cyclohexen-1-yl)-, acetate

    Cas No: 103905-07-3

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103905-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103905-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,9,0 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103905-07:
(8*1)+(7*0)+(6*3)+(5*9)+(4*0)+(3*5)+(2*0)+(1*7)=93
93 % 10 = 3
So 103905-07-3 is a valid CAS Registry Number.

103905-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-acetoxy-3,7-dimethyl-8-(tetrahydropyran-2-yl)oxy-9-phenylsulfonyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2(E),6(E)-nonadiene

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:103905-07-3 SDS

103905-07-3Relevant articles and documents

Process for producing vitamin A or its carboxylic acid esters, and intermediate compounds useful for the process

-

, (2008/06/13)

A process for producing vitamin A represented by the formula STR1 which comprises treating a compound represented by the formula STR2 wherein R1 represents an aryl group which may be substituted, R21 and R22 each represents a hydrogen atom or a lower alkanoyl group, R3 represents an acetal-type protective group for a hydroxyl group, and X represents a halogen atom, with a base; and novel intermediate compounds useful for the above process.

THE HIGHLY STEREOSELECTIVE SYNTHESIS OF ALL-TRANS AND 13-CIS VITAMIN A VIA DOUBLE ELIMINATION REACTION

Otera, Junzo,Misawa, Hiromitsu,Mandai, Tadakatsu,Onishi, Takashi,Suzuki, Shigeaki,Fujita, Yoshiji

, p. 1883 - 1886 (2007/10/02)

Stereocontrolled convergent synthesis of vitamin A was achieved by the double elimination method employing the C10 sulfone and the C10 aldehydes as starting materials.Thus the all-trans and 13-cis isomers were obtained with the stereochemical purity of 95percent and 90percent, respectively.

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