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1073-73-0

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1073-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1073-73-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1073-73:
(6*1)+(5*0)+(4*7)+(3*3)+(2*7)+(1*3)=60
60 % 10 = 0
So 1073-73-0 is a valid CAS Registry Number.

1073-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(oxolan-2-yl)propan-2-one

1.2 Other means of identification

Product number -
Other names 2-furyl acetone

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:1073-73-0 SDS

1073-73-0Downstream Products

1073-73-0Relevant articles and documents

A Free-Radical Acetonylation Method

Jaouhari, Rabih,Maillard, Bernard,Filliatre, Claude,Villenave, Jean-Jacques

, p. 760 - 763 (1982)

-

Radical addition of ethers to alkenes under dioxygen catalyzed by N-hydroxyphthalimide (NHPI)/Co(OAc)2

Hirano, Kazutaka,Sakaguchi, Satoshi,Ishii, Yasutaka

, p. 3617 - 3620 (2002)

The reaction of various ethers with alkenes bearing an electron-withdrawing substituent in the presence of N-hydroxyphthalimide combined with Co(OAc)2 under dioxygen produced the corresponding adducts in which oxygen is incorporated to alkenes

Thiourea/proline derivative-catalyzed synthesis of tetrahydrofuran derivatives: A mechanistic view

Opalka, Suzanne M.,Steinbacher, Jeremy L.,Lambiris, Brandon A.,McQuade, D. Tyler

experimental part, p. 6503 - 6517 (2011/10/02)

A thiourea/proline derivative-catalyzed synthesis of linear α-substituted tetrahydrofuran/pyran derivatives starting with lactol substrates is presented. This study demonstrates the utility and potential complications of using (thio)urea/proline cocatalysis as each of these catalysts is necessary to provide the observed reactivity, but a time-dependent decrease in enantioselectivity is observed. New mechanistic insights into (thio)urea/proline cocatalysis are presented.

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