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Furan, tetrahydro-2-methoxy-5-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138745-73-0

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138745-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138745-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138745-73:
(8*1)+(7*3)+(6*8)+(5*7)+(4*4)+(3*5)+(2*7)+(1*3)=160
160 % 10 = 0
So 138745-73-0 is a valid CAS Registry Number.

138745-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzenesulfonyl)-5-methoxyoxolane

1.2 Other means of identification

Product number -
Other names 2-methoxy-5-phenylsulfonyltetrahydrofuran

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:138745-73-0 SDS

138745-73-0Relevant academic research and scientific papers

Lactol PAF antagonists

-

, (2008/06/13)

The invention encompasses compounds of general formula I: STR1 wherein W represents an imidazo[4,5-c]pyridyl group, optionally substituted with one or more substituents selected from C1 -C6 alkyl, C1 -C6 alkoxy, halo, CF, and CN; and Z, R1, R2, R3, R4, R5, R6 are variables. These compounds are useful as antagonists of platelet activating factor.

SUBSTITUTION REACTIONS OF 2-BENZENESULPHONYL CYCLIC ETHERS WITH CARBON NUCLEOPHILES

Brown, Dearg S.,Bruno, Maurizio,Davenport, Raymond J.,Ley, Steven V.

, p. 4293 - 4308 (2007/10/02)

Direct substitution of 2-benzenesulphonylcyclic ethers was studied using a variety of carbon nucleophiles.These nucleophiles included organozinc reagents (derived from aryl, vinyl and alkynyl Grignard reagents) or silyl enol ethers, silyl ketene acetals,

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