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1-Propanol, 2-phenoxy-, 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69333-61-5

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69333-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69333-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,3 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69333-61:
(7*6)+(6*9)+(5*3)+(4*3)+(3*3)+(2*6)+(1*1)=145
145 % 10 = 5
So 69333-61-5 is a valid CAS Registry Number.

69333-61-5SDS

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 4-methylbenzenesulfonic acid,2-phenoxypropan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Propanol,2-phenoxy-,4-methylbenzenesulfonate

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:69333-61-5 SDS

69333-61-5Downstream Products

69333-61-5Relevant academic research and scientific papers

Novel juvenoids of the 2-(4-hydroxybenzyl)cyclohexan-1-one series

Wimmer,Saman,Francke

, p. 502 - 508 (2007/10/02)

A series of insect juvenile hormone analogs (juvenoids) was synthesized and studied. The basic skeleton of these juvenoids contains three rings and a short aliphatic subunit and bears two or three chiral centers (depending on the appropriate structure; see 6-9). The chiral center located in the 1,2-diphenoxypropane subunit has the configuration (RS), (R) (a series), or (S) (b series). The juvenoids were subjected to a biological screening, the preliminary results of which are briefly described.

Asymmetric hydrogenation catalyzed by rhodium complexes of chiral tertiary phosphines

-

, (2008/06/13)

A method for the homogeneous catalytic enantioselective hydrogenation of alkyl and alkenyl substituted acrylic acids wherein these acids are selectively hydrogenated at the double bond alpha, beta to the acid function, said hydrogenations are catalyzed by

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