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805228-93-7

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805228-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 805228-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,5,2,2 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 805228-93:
(8*8)+(7*0)+(6*5)+(5*2)+(4*2)+(3*8)+(2*9)+(1*3)=157
157 % 10 = 7
So 805228-93-7 is a valid CAS Registry Number.

805228-93-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL Z-BROMO-(DIHYDROFURAN-2-YLIDENE)ACETATE

1.2 Other means of identification

Product number -
Other names -

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:805228-93-7 SDS

805228-93-7Relevant articles and documents

Synthesis of benzofurans with remote bromide functionality by domino "ring-cleavage-deprotection-cyclization" reactions of 2-alkylidenetetrahydrofurans with boron tribromide

Bellur, Esen,Langer, Peter

, p. 7686 - 7693 (2007/10/03)

Bromination and subsequent Suzuki reactions of 2- alkylidenetetrahydrofurans, readily available by [3+2] cyclizations, afforded 1′-(2″-methoxyphenyl)-2-alkylidenetetrahydrofurans. Treatment of the latter with boron tribromide and subsequent addition of wa

Functionalization of 2-alkylidenetetrahydrofurans and 2- alkylidenepyrrolidines by palladium(0)-catalyzed cross-coupling reactions

Bellur, Esen,Langer, Peter

, p. 2169 - 2171 (2007/10/03)

2-Alkylidenetetrahydrofurans and 2-alkylidenepyrrolidines were efficiently functionalized by bromination of the exocyclic double bond and subsequent palladium-catalyzed cross-coupling reactions.

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