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3-Penten-2-one, 4-(methylthio)-, (3E)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86310-01-2

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86310-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86310-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,1 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86310-01:
(7*8)+(6*6)+(5*3)+(4*1)+(3*0)+(2*0)+(1*1)=112
112 % 10 = 2
So 86310-01-2 is a valid CAS Registry Number.

86310-01-2SDS

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 (E)-4-methylsulfanyl-3-penten-2-one

1.2 Other means of identification

Product number -
Other names (E)-4-methylhiopent-3-en-2-one

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:86310-01-2 SDS

86310-01-2Downstream Products

86310-01-2Relevant academic research and scientific papers

New ketone homoenolate anion equivalents derived from (alkenyl)pentamethyl phosphoric triamides

Grison, Claude,Thomas, Antoine,Coutrot, Frédéric,Coutrot, Philippe

, p. 2101 - 2123 (2007/10/03)

Lithiated ambident anions derived from (1-alkyl-2-propenyl)- or (1-phenyl-2-propenyl)-pentamethyl phosphoric triamides undergo regioselectively γ-reaction with various alkylating reagents and isobutyraldehyde. Further hydrolysis of adducts releases the ketone under acid conditions. Number of synthetic applications clearly show the ketone homoenolate behaviour of these new carbanions.

Stereoselectivity in the Addition of Organocuprates to β-Alkylthio α,β-Enones

Dieter, R. Karl,Silks, Louis A.

, p. 2786 - 2788 (2007/10/02)

Factors affecting the direction and degree of stereoselectivity in the conjugate addition-elimination reaction of organocuprates with β-alkylthio α,β-enones are described.

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