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3739-97-7

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3739-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3739-97-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,3 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3739-97:
(6*3)+(5*7)+(4*3)+(3*9)+(2*9)+(1*7)=117
117 % 10 = 7
So 3739-97-7 is a valid CAS Registry Number.

3739-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(trimethylsilylmethylidene)-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names triphenyl(trimethylsilylmethylidene)

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:3739-97-7 SDS

3739-97-7Relevant articles and documents

Total synthesis of echinopines A and B: Exploiting a bioinspired late-stage intramolecular cyclopropanation

Peixoto, Philippe A.,Richard, Jean-Alexandre,Severin, Rene,Chen, David Y.-K.

supporting information; experimental part, p. 5724 - 5727 (2011/12/15)

Total synthesis of echinopine A and B have been accomplished, based on a strategy that involved two transition-metal-mediated ene-yne cycloisomerizations. A modified Pd-catalyzed enyne cycloisomerization/ intramolecular Diels-Alder cascade rendered a more

Stabilized and persistent allenylketenes

Huang, Wenwei,Fang, Decai,Temple, Karen,Tidwell, Thomas T.

, p. 2832 - 2838 (2007/10/03)

Photolyses of 2,3-bis(trimethylsilyl)-substituted methylenecyclobutenones 22-26 give essentially quantitative conversion to the allenylketenes 28-32 which have been isolated as long-lived species at room temperature. As predicted by molecular orbital calc

Synthesis and reactions of [1-(trialkylsilyl)alkylidene]triphenylphosphoranes

Bestmann,Bomhard,Dostalek,Pichl,Riemer,Zimmermann

, p. 787 - 792 (2007/10/02)

Alkylidenetriphenylphosphoranes 1 react with trialkyl halosilanes 2 to afford silylated alkylidenephosphoranes 5, which can be converted to acylated alkylidenephosphoranes 8 and 10 by trimethylsilyl carboxylates 6 or carboxylic anhydrides 10. Bis(acylalkylidenephosphoranes) 13-15 are available from 5 and bis(trimethylsilyl) dicarboxylates 12 or cyclic or polymeric anhydrides 16, 17.

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