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1,2,3-Propanetriol, 2-(4-methylbenzenesulfonate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73684-56-7

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73684-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73684-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,8 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73684-56:
(7*7)+(6*3)+(5*6)+(4*8)+(3*4)+(2*5)+(1*6)=157
157 % 10 = 7
So 73684-56-7 is a valid CAS Registry Number.

73684-56-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-p-toluenesulfonyloxy-1,3-propanediol

1.2 Other means of identification

Product number -
Other names 2-tosyloxy-1,3-propanediol

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:73684-56-7 SDS

73684-56-7Relevant academic research and scientific papers

New technology for synthesizing 1,3-propylene glycol from glycerin through dehydroxylation method

-

Paragraph 0023, (2017/05/12)

The invention discloses a new technology for synthesizing 1,3-propylene glycol from glycerin through a dehydroxylation method. The technology comprises the following steps: protecting two hydroxyl groups at the head end and the tail end of a glycerin molecule through using a group protection process, converting a hydroxyl group in the middle of the molecule into a group easy to eliminate, that is a sulfonyloxy group, removing hydroxyl group protection groups, and reducing the sulfonyloxy in the presence of a catalyst in order to obtain the 1,3-propylene glycol product. The technology has the characteristics of few byproducts, easiness in separation, and low cost, is a route with environmentally-friendly and economic dual values, and has wide development prospect.

Triazole antifungal agent

-

, (2008/06/13)

A triazole compound having the formula: STR1 wherein Ar1 represents an optionally substituted phenyl, Ar2 represents an optionally substituted phenyl, R0 represents a hydrogen atom or a lower alkyl; R1 represents a lower alkyl; R2 to R5 represent a hydrogen atom or an unsubstituted or halo substituted alkyl, n represents 0 to 2; p represents 0 or 1; q, r and s each represent 0 to 2; and A represents a 1,3-dioxan-5-yl. The triazole compound of the present invention exhibits an excellent antifungal activity.

Structure-activity relationship of lipopeptide from outer membrane of Escherichia coli and synthesis of highly immunopotenting lipopeptide derivatives with an achiral lipo-part

Kurimura,Achiwa

, p. 627 - 629 (2007/10/02)

For outstanding the structure-activity relationship of lipopeptide derivatives, high biologically active lipopeptide derivatives with an achiral lipo-part were newly synthesized.

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