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20826-94-2

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20826-94-2 Usage

Chemical Properties

Clear colorless to yellowish liquid

Uses

Ethyl 2-oxocyclopentylacetate is used as an organic chemical synthesis intermediate.

Synthesis Reference(s)

Journal of the American Chemical Society, 99, p. 5222, 1977 DOI: 10.1021/ja00457a075Tetrahedron, 52, p. 9713, 1996 DOI: 10.1016/0040-4020(96)00511-X

Check Digit Verification of cas no

The CAS Registry Mumber 20826-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,2 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20826-94:
(7*2)+(6*0)+(5*8)+(4*2)+(3*6)+(2*9)+(1*4)=102
102 % 10 = 2
So 20826-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O3/c1-2-12-9(11)6-7-4-3-5-8(7)10/h7H,2-6H2,1H3

20826-94-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H61589)  Ethyl 2-oxocyclopentylacetate, 95%   

  • 20826-94-2

  • 5g

  • 1497.0CNY

  • Detail
  • Alfa Aesar

  • (H61589)  Ethyl 2-oxocyclopentylacetate, 95%   

  • 20826-94-2

  • 25g

  • 5992.0CNY

  • Detail

20826-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2-oxocyclopentyl)acetate

1.2 Other means of identification

Product number -
Other names 2-Oxocyclopentaneacetic Acid Ethyl Ester

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:20826-94-2 SDS

20826-94-2Relevant articles and documents

Free-radical-mediated Carbonylative Cyclization of Alk-4-enyl Halides Leading to Cyclopentanone

Ryu, Ilhyong,Kusano, Kazuya,Hasegawa, Mitsuharu,Kambe, Nobuaki,Sonoda, Noboru

, p. 1018 - 1019 (2007/10/02)

Alk-4-enyl bromides and iodides 1, when treated with the tributyltin hydride/CO sustem, undergo carbonylative cyclization to give cyclopentanones in good yields (AIBN cat., benzene, 79-90 atm, = 0.025-0.05 mol dm-3, 80 deg C.

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