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10433-88-2

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10433-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10433-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,3 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10433-88:
(7*1)+(6*0)+(5*4)+(4*3)+(3*3)+(2*8)+(1*8)=72
72 % 10 = 2
So 10433-88-2 is a valid CAS Registry Number.

10433-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-methyl-2-(3-oxobutyl)propanedioate

1.2 Other means of identification

Product number -
Other names 5,5-dicarbethoxy-2-hexanone

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:10433-88-2 SDS

10433-88-2Relevant articles and documents

NUCLEOPHILIC RING OPENING OF DIETHYL 1,1-CYCLOPROPANEDICARBOXYLATE USING Na2Fe(CO)4*3/2 DIOXANE

Tamblyn, William H.,Waltermire, Robert E.

, p. 2803 - 2806 (1983)

Diethyl 1,1-cyclopropanedicarboxylate undergoes nucleophilic ring opening with Na2Fe(CO)4*3/2 dioxane under CO at room temperature to produce a variety of carbonylated products.

BENZOQUINOLONE INHIBITORS OF VMAT2

-

Paragraph 00117; 00118, (2015/04/15)

The present invention relates to new benzoquinolone inhibitors of VMAT2, pharmaceutical compositions thereof, and methods of use thereof represented by structural Formula I.

BENZOQUINOLINE INHIBITORS OF VESICULAR MONOAMINE TRANSPORTER 2

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Paragraph 00184; 00185, (2015/06/08)

The present invention relates to new benzoquinoline inhibitors of vesicular monoamine transporter 2 (VMAT2), pharmaceutical compositions thereof, and methods of use thereof. (I)

Phosphine-boronates: Efficient bifunctional organocatalysts for Michael addition

Basle, Olivier,Porcel, Susana,Ladeira, Sonia,Bouhadir, Ghenwa,Bourissou, Didier

supporting information; experimental part, p. 4495 - 4497 (2012/05/31)

Phosphine-boronates R2P(o-C6H4) B(OR′)2 have been evaluated as bifunctional organocatalysts for the Michael addition of malonate pronucleophiles to methylvinylketone. The presence of the Lewis acidic boron center adjacent to phosphorus significantly improves catalytic performance. Isolation and complete characterization of a key intermediate, namely a β-phosphonium enolate, substantiate the role of the Lewis acidic moiety in the catalytic process.

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