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(+/-)-methyl 3-(tert-butyldiphenylsilyloxy)-2-hydroxypropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

173105-57-2

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173105-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173105-57-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,1,0 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 173105-57:
(8*1)+(7*7)+(6*3)+(5*1)+(4*0)+(3*5)+(2*5)+(1*7)=112
112 % 10 = 2
So 173105-57-2 is a valid CAS Registry Number.

173105-57-2Relevant academic research and scientific papers

Antibody drug conjugate, intermediate, preparation method, pharmaceutical composition and uses thereof

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Page/Page column 189; 190; 191, (2019/11/11)

Disclosed are an antibody drug conjugate IB, which uses ether linkages for connection, and improves the water solubility, stability and cytotoxicity in vivo and in intro, and an intermediate, a pharmaceutical composition, and uses of the antibody drug conjugate. The antibody drug conjugate has simple synthetic steps and a high yield.

Kinetic resolution of racemic carboxylic acids by an L-histidine-derived sulfonamide-induced enantioselective esterification reaction

Ishihara, Kazuaki,Kosugi, Yuji,Umemura, Shuhei,Sakakura, Akira

supporting information; experimental part, p. 3191 - 3194 (2009/05/27)

(Chemical Equation Presented) The direct and catalytic kinetic resolution of racemic carboxylic acids bearing a Bronsted base such as O-protected α-hydroxy carboxylic acids and N-protected α-amino acids has been accomplished through an L-histidine-derived sulfonamide-induced enantioselective esterification reaction with tert-butyl alcohol for the first time. Highly asymmetric induction [S(kfast/kslow) = up to 56] has been achieved under the equilibrium between a chiral catalyst and two diastereomeric acylammonium salts through an intramolecular hydrogen-bonding interaction.

Anti-viral compounds

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, (2008/06/13)

Nucleotide analogues having the general formula (I) and pharmaceutically acceptable derivatives: STR1 wherein n is 0 or an integer; X is O or S, CH2, CH-halogen, CH--N3, or C=CH2 ; Q and U are independently selected from: O, S, and CH(Ra) wherein Ra is hydrogen, OH, halogen, N3, NH2, SH, carboxyl, C1-6 alkyl or Ra is CH2 (Rb) wherein Rb is hydrogen, OH, SH, NH2, C1-6 alkyl or carboxyl; or both Q and U are CH when Q and U are linked by a double bond; Z is selected from: O, a C1-6 alkoxy, a C1-6 thioalkyl, a C1-6 aminoalkyl, (CH2)m wherein m is 0 or an integer, and N(Rc)2 wherein both Rc are independently hydrogen or a C1-6, alkyl; and R2 is a purine or pyrimidine base or an analogue or derivative thereof are disclosed. Members of this series of analogues possess anti-viral activity.

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