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37627-42-2

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37627-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37627-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,2 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 37627-42:
(7*3)+(6*7)+(5*6)+(4*2)+(3*7)+(2*4)+(1*2)=132
132 % 10 = 2
So 37627-42-2 is a valid CAS Registry Number.

37627-42-2SDS

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 (Z)-3-(3,4-dimethoxyphenyl)acrylonitrile

1.2 Other means of identification

Product number -
Other names cis-β-(3,4-Dimethoxyphenyl)-acrylnitril

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:37627-42-2 SDS

37627-42-2Downstream Products

37627-42-2Relevant articles and documents

Synthesis and Catalytic Use of Gold(I) Complexes Containing a Hemilabile Phosphanylferrocene Nitrile Donor

?koch, Karel,Císa?ová, Ivana,?těpni?ka, Petr

supporting information, p. 15998 - 16004 (2015/11/03)

Removal of the chloride ligand from [AuCl(1-κP)] (2) containing a P-monodentate 1′-(diphenylphosphanyl)-1-cyanoferrocene ligand (1), by using silver(I) salts affords cationic complexes of the type [Au(1)]X, which exist either as cyclic dimers [Au(1)]2X2 (3a, X=SbF6; 3 c, X=NTf2) or linear coordination polymers [Au(1)]nXn (3 a′, X=SbF6; 3 b′, X=ClO4), depending on anion X and the isolation procedure. As demonstrated for 3 a′, the polymers can be readily cleaved by the addition of donors, such as Cl-, tetrahydrothiophene (tht) or 1, giving rise to the parent compound 2, [Au(tht)(1-κP)][SbF6] (5 a) or [Au(1-κP)2][SbF6] (4 a), respectively, of which the last two compounds can also be prepared by stepwise replacement of tht in [Au(1-κP)2][SbF6]. The particular combination of a firmly coordinated (phosphane) and a dissociable (nitrile) donor moieties renders complexes 3/3′ attractive for catalysis because they can serve as shelf-stable precursors of coordinatively unsaturated AuI fragments, analogous to those that result from the widely used [Au(PR3)(RCN)]X catalysts. The catalytic properties of the Au-1 complexes were evaluated in model annulation reactions, such as the synthesis of 2,3-dimethylfuran from (Z)-3-methylpent-2-en-4-yn-1-ol and oxidative cyclisation of alkynes with nitriles to produce 2,5-disubstituted 1,3-oxazoles. Of the compounds tested (2, 3 a′, 3 b′, 3 a, 4 a and 5 a), the best results were consistently achieved with dimer 3 c, which has good solubility in organic solvents and only one firmly bound donor at the gold atom. This compound was advantageously used in the key steps of annuloline and rosefuran syntheses.

Total synthesis of (+)-virgatusin via AlCl3-catalyzed [3+2] cycloaddition

Sanders, Shanina D.,Ruiz-Olalla, Andrea,Johnson, Jeffrey S.

supporting information; experimental part, p. 5135 - 5137 (2009/12/08)

The AlCl3-catalyzed cycloaddition of a donor-acceptor (don-acc) cyclopropane and piperonal succinctly provides the core of virgatusin in a selective, high-yielding manner. The Royal Society of Chemistry 2009.

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