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1636-01-7

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1636-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1636-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1636-01:
(6*1)+(5*6)+(4*3)+(3*6)+(2*0)+(1*1)=67
67 % 10 = 7
So 1636-01-7 is a valid CAS Registry Number.

1636-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name oxovanadium,propan-2-ol,dihydrochloride

1.2 Other means of identification

Product number -
Other names 2-Propanol,vanadium complex

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:1636-01-7 SDS

1636-01-7Relevant articles and documents

Oxovanadium(v)-catalyzed oxidative cross-coupling of enolates using O2as a terminal oxidant

Osafune, Yuma,Jin, Yuqing,Hirao, Toshikazu,Tobisu, Mamoru,Amaya, Toru

supporting information, p. 11697 - 11700 (2020/10/19)

The oxovanadium(v)-catalyzed oxidative cross-coupling of enolates using O2 as a terminal oxidant is reported, where a boron enolate and a silyl enol ether were employed as enolates. The redox behavior of V(v/iv) in this reaction under O2 was investigated by ESR and 51V NMR experiments.

High valence vanadium complex promoted selective rearrangement of epoxides to aldehydes or ketones

Martinez, Fernando,Campo, Carmen del,Llama, Emilio F.

, p. 1749 - 1752 (2008/10/08)

High valence vanadium complexes induce the selective ring opening of epoxides. The monosubstituted epoxides are isomerized with complete regioselectivity each forming a single carbonyl compound exclusively. Likewise a highly regioselective isomerization of 1,1-disubstituted or 1,1,2-trisubstituted epoxides was observed in all reactions.

Functionalized Oxovanadium Alkoxides - Potential Haptens

Hillerns, Frank,Rehder, Dieter

, p. 2249 - 2254 (2007/10/02)

Several new oxovanadium alkoxides and alkoxides/chlorides of the composition VOCl3-n(OR)n (n = CPh3; n = 2 and 3, R = CPh3, iBu, cyclopentyl, tert-pentyl, octyl; n 3, R = dodecyl, 3-methylbutyl) and the mixed ester VO(OiBu)-(OCPh3)2 have been prepared.The compounds VO(OiBu)2OR' have ben synthesized, where R' is a functionalized long-chain alkyl group .The chloride/carboxylate VOCl2 has also been obtained.The compounds are characterized, inter alia, by 51V-NMR spectroscopy.Typical 51V shift ranges are observed for specific ligand functionalities (chlorides, alkoxide, carboxylate). δ(51V) values also depend on the steric requirement of the groups R and the coordination number.The importance of the functionalized esters as potential triggers for the production of abzymes with phosphatase activity is discussed.Key Words: Vanadium Alkoxides / Haptens / NMR, 51V

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