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159146-89-1

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159146-89-1 Usage

Chemical Class

Enones

Physical State

Yellow liquid

Odor

Strong

Solubility

Slightly soluble in water

Common Uses

Intermediate in pharmaceutical and agrochemical synthesis
Production of flavor and fragrance compounds

Hazards

Skin and eye irritation upon contact
Harmful if swallowed or inhaled

Safety Precautions

Proper handling and storage measures are necessary

Check Digit Verification of cas no

The CAS Registry Mumber 159146-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,1,4 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 159146-89:
(8*1)+(7*5)+(6*9)+(5*1)+(4*4)+(3*6)+(2*8)+(1*9)=161
161 % 10 = 1
So 159146-89-1 is a valid CAS Registry Number.

159146-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name hex-4-yne-2,3-dione

1.2 Other means of identification

Product number -
Other names 4-Hexyne-2,3-dione (9CI)

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:159146-89-1 SDS

159146-89-1Downstream Products

159146-89-1Relevant articles and documents

Photoaddition of alkenes to conjugated α-diketones: Tandem cyclizations leading to tetrasubstituted furans

Mukherjee,Margaretha,Agosta

, p. 3388 - 3391 (2007/10/03)

Photocycloaddition of 9a-c with 2 leads cleanly to tetrasubstituted furans 12a-c, respectively, in yields of ~85%. The reactive triplet is efficiently sensitized by 2-benzoylnaphthalene and quenched by anthracene, indicating that E(T) is in the range 43-58 kcal/mol. A mechanism is proposed involving an alkyl propargyl biradical (as 10) that closes first to a vinyl carbene (as 11) and then to product. Reaction of 9c with 20 furnishes only 22, and this result rules out an alternative mechanism in which the order of steps leading to the carbene is reversed.

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