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1217254-25-5

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1217254-25-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1217254-25-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,2,5 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1217254-25:
(9*1)+(8*2)+(7*1)+(6*7)+(5*2)+(4*5)+(3*4)+(2*2)+(1*5)=125
125 % 10 = 5
So 1217254-25-5 is a valid CAS Registry Number.

1217254-25-5Upstream product

1217254-25-5Downstream Products

1217254-25-5Relevant articles and documents

Asymmetric microbial reduction of ketones: absolute configuration of trans-4-ethyl-1-(1S-hydroxyethyl)cyclohexanol

Pinedo-Rivilla, Cristina,Cafeu, Mariana Carrara,Casatejada, Josefina Aleu,Araujo, Angela Regina,Collado, Isidro G.

experimental part, p. 2666 - 2672 (2010/05/17)

A set of five fungal species, Botrytis cinerea, Trichoderma viride and Eutypa lata, and the endophytic fungi Colletotrichum crassipes and Xylaria sp., was used in screening for microbial biocatalysts to detect monooxygenase and alcohol dehydrogenase activities (for the stereoselective reduction of carbonyl compounds). 4-Ethylcyclohexanone and acetophenone were biotransformed by the fungal set. The main reaction pathways involved reduction and hydroxylations at several positions including tertiary carbons. B. cinerea was very effective in the bioreduction of both substrates leading to the chiral alcohol (S)-1-phenylethanol in up to 90% enantiomeric excess, and the cis-trans ratio for 4-ethylcyclohexanol was 0:100. trans-4-Ethyl-1-(1S-hydroxyethyl)cyclohexanol, obtained from biotransformation by means of an acyloin-type reaction, is reported here for the first time. The absolute configurations of the compounds trans-4-ethyl-1-(1S-hydroxyethyl)cyclohexanol and 4-(1S- and 4-(1R-hydroxyethyl)cyclohexanone were determined by NMR analysis of the corresponding Mosher's esters.

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