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Ethanone, 1-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-[[(1,1-dimethylethyl)diphenylsil yl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147107-70-8

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147107-70-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147107-70-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,0 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147107-70:
(8*1)+(7*4)+(6*7)+(5*1)+(4*0)+(3*7)+(2*7)+(1*0)=118
118 % 10 = 8
So 147107-70-8 is a valid CAS Registry Number.

147107-70-8Downstream Products

147107-70-8Relevant academic research and scientific papers

A rapid synthesis of hexofuranose-like iminosugars using ring-closing metathesis

Cren, Sylvaine,Wilson, Claire,Thomas, Neil R.

, p. 3521 - 3523 (2005)

(Chemical Equation Presented) Two new 1-N-iminosugars have been prepared as hexofuranose analogues in an efficient manner by an RCM-based route. Both 3,4-disubstituted pyrrolidines display moderate inhibitory activity against Mycobacterium smegmatis galac

Synthetic study of cnicin: Synthesis of the side chain and its esterification

Kurita, Manami,Tanigawa, Miho,Narita, Shuhei,Usuki, Toyonobu

, p. 5899 - 5901 (2016)

Cnicin is a germacranolide sesquiterpene lactone that possesses potent inhibitory activity against the protozoan parasite Trypanosoma brucei, which causes human African trypanosomiasis (HAT). Although cnicin has an interesting structure and attractive biological activity, synthetic studies of cnicin have not yet been reported. This report describes the synthesis of the protected side chain carboxylic acid moiety at C8 of cnicin via two routes starting from L-ascorbic acid. In addition, esterification between the synthetic side chain and salonitenolide derivative, which can be achieved via hydrolysis of cnicin and protection of the primary alcohol, was conducted. Thus, a semi-synthesis of cnicin was achieved.

An efficient preparation of silylated derivatives of L-erythrulose 3,4- O-acetals

Carda,Rodriguez,Murga,Falomir,Marco,Roeper

, p. 2601 - 2610 (2007/10/03)

An efficient and reproducible procedure for the preparation of 1-O- silylated derivatives of several 3,4-O-acetals of erythrulose from the parent sugar is described.

Synthesis of protected enantiopure erythrulose derivatives

Marco, J. Alberto,Carda, Miguel,Gonzalez, Florenci,Rodriguez, Santiago,Murga, Juan

, p. 1801 - 1810 (2007/10/03)

D- and L-Erythrulose derivatives 2-6 bearing protective O-silyl and O-benzyl groups in various positions were synthesized in enantiopure form from L-ascorbic acid, D-isoascorbic acid, and D-glucose. VCH Verlagsgesellschaft mbH, 1996.

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