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17692-20-5

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17692-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17692-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17692-20:
(7*1)+(6*7)+(5*6)+(4*9)+(3*2)+(2*2)+(1*0)=125
125 % 10 = 5
So 17692-20-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O3/c1-10(13,7-9(11)12)8-5-3-2-4-6-8/h8,13H,2-7H2,1H3,(H,11,12)

17692-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Cyclohexyl-3-hydroxybutanoic acid

1.2 Other means of identification

Product number -
Other names Acido cyclobutoico

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:17692-20-5 SDS

17692-20-5Downstream Products

17692-20-5Relevant academic research and scientific papers

A convenient generation of acetic acid dianion

Parra, Margarita,Sotoca, Enrique,Gil, Salvador

, p. 1386 - 1388 (2007/10/03)

The lithium enediolate of acetic acid can be generated efficiently, as a 0.5 M solution in THF, using lithium amides prepared from n-butyllithium in THF and either diethylamine or 1,3,3-trimethyl-6-azabicyclo-(3.2.1)-octane (AZA). Its reaction with carbon

Synthesis of 3-Hydroxy-3-cyclohexylbutyric Acid Derivatives. 2. Cyclic Analogues of Mevalonic Acid

Carganico, Germano,Cozzi, Paolo,Orsini, Gaetano

, p. 1767 - 1769 (2007/10/02)

The sodium salt of (Z)-3-hydroxy-3-(2-hydroxycyclohexyl)butyric acid (I) and its lactone (II) were prepared through the corresponding tert-butyl ester by hydrogenation, over Rh/Al2O3 catalyst, of the phenyl ring of tert-butyl 3-hydroxy-3-(2-hydroxyphenyl)butyrate (III). (Z)-3-Hydroxy-3-(2-methoxycyclohexyl)butyric acid was prepared similarly. (Z)-4-Methyloctahydro-2H-1-benzopyran-2-one was prepared by hydrogenation, over Rh/Al2O3 catalyst, of 4-methylcoumarine, prepared in turn from III by a one-pot procedure comprising hydrolysis, lactonization, and dehydration.The above compounds inhibit acetate incorporation in cholesterol and fatty acids in rat liver slices at 5 * 10-3 M, but they lack specific inhibitory activity on HMG-CoA reductase.

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