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4-Cyclopentyl-4-oxo-butyric acid is a chemical compound with the molecular formula C9H14O3. It is a white crystalline solid that is soluble in organic solvents. 4-CYCLOPENTYL-4-OXO-BUTYRIC ACID is a derivative of cyclopentyl and butyric acid, featuring a cyclopentyl group attached to a 4-oxo-butyric acid moiety. It is used in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the development of drugs targeting the central nervous system. Due to its unique structure, it has potential applications in the creation of novel therapeutic agents and as a building block in organic chemistry.

3400-90-6

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3400-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3400-90-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3400-90:
(6*3)+(5*4)+(4*0)+(3*0)+(2*9)+(1*0)=56
56 % 10 = 6
So 3400-90-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O3/c10-8(5-6-9(11)12)7-3-1-2-4-7/h7H,1-6H2,(H,11,12)

3400-90-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-cyclopentyl-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names 4-oxo-4-cyclopentylbutanoic acid

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:3400-90-6 SDS

3400-90-6Relevant academic research and scientific papers

Synthesis of γ-, δ-, and ε-lactams by asymmetric transfer hydrogenation of N-(tert-butylsulfinyl)iminoesters

Guijarro, David,Pablo, Oscar,Yus, Miguel

, p. 3647 - 3654 (2013/05/22)

Highly enantiomerically enriched γ- and δ-lactams have been prepared by a simple and very efficient procedure that involves the asymmetric transfer hydrogenation of N-(tert-butylsulfinyl)iminoesters followed by desulfinylation of the nitrogen atom and spo

Efficient regioselective oxetane formation during photochemical transformation of spiro[4. n]-2,5-Diones

Sudini, Ravinder R.,Saravanan,Kumar, Pradeep

, p. 3263 - 3273 (2007/10/03)

The irradiation of a variety of spirodiones (3) in the presence of carbonyl compounds led to the formation of oxetanes (6) regioselectively, which upon hydrolysis afforded the corresponding ketoacids (7) in excellent yields.

4-(trans-4-methylcyclohexyl)-4-oxobutyric acid (JTT-608). A new class of antidiabetic agent

Shinkai, Hisashi,Ozeki, Hidekazu,Motomura, Takahisa,Ohta, Takeshi,Furukawa, Noboru,Uchida, Itsuo

, p. 5420 - 5428 (2007/10/03)

During an investigation of drugs for improving the β-cell response to glucose, we found that 4-cyclohexyl-4-oxobutyric acid selectively improved glucose-stimulated insulin release and glucose tolerance in both normal and diabetic rats. A series of 4-cyclo

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