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(1S,3R,4S,5R,6R)-4,5-Bis-benzyloxy-3-benzyloxymethyl-7,7-dichloro-2-oxa-bicyclo[4.1.0]heptane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

162332-13-0

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162332-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162332-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,3 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 162332-13:
(8*1)+(7*6)+(6*2)+(5*3)+(4*3)+(3*2)+(2*1)+(1*3)=100
100 % 10 = 0
So 162332-13-0 is a valid CAS Registry Number.

162332-13-0Relevant articles and documents

Cytotoxic effects of C-glycosides in HOS and HeLa cell lines

Sanhueza, Carlos A.,Mayato, Carlos,Machin, Ruben P.,Padron, Jose M.,Dorta, Rosa L.,Vazquez, Jesus T.

, p. 3676 - 3681 (2008/02/05)

Fifty-two C-glycosides were synthesized and their in-vitro antiproliferative activity screened against human cervical carcinoma (HeLa) and osteosarcoma (HOS) cell lines. Nine of them had growth inhibitions (GI50 values) below 10 μM, the C-gluco

A new procedure for highly regio- and stereoselective iodoacetoxylation of protected glycals and α-1,2-cyclopropanated sugars

Gammon, David W.,Kinfe, Henok H.,De Vos, Dirk E.,Jacobs, Pierre A.,Sels, Bert F.

, p. 141 - 157 (2008/02/11)

Protected glycals and -1,2-cyclopropanated sugars were converted in high yields and selectivities in less than 2h at low temperatures to 2-deoxy-2-iodoglycosyl acetates or novel 2-deoxy-2-iodomethylglycosyl acetates using the simple, inexpensive reagent m

Studies towards the synthesis of the C29-C51 fragment of altohyrtin A

Fernandez-Megia, Eduardo,Gourlaouen, Nelly,Ley, Steven V.,Rowlands, Gareth J.

, p. 991 - 994 (2007/10/03)

The synthesis of the highly substituted E and F pyran fragment 23 of altohyrtin A 1 from tri-O-benzyl-D-glucal 5 is described. The synthesis of a model compound 31 containing the altohyrtin A triene side-chain outlines the proposed strategy for the elabor

Synthesis and Reactions of 1,2-Cyclopropanated Sugars

Ramana,Murali,Nagarajan

, p. 7694 - 7703 (2007/10/03)

Diastereospecific cyclopropanation of glycals 1, 2, 3, 4, and 41 was carried out using either dihalocarbene addition or zinc-carbenoid addition to yield 1,2-cyclopropanated sugars. Dichloroand dibromocarbenes added stereoselectively anti to the C3/s

Synthesis of 1,2-Cyclopropanated Sugars from Glycals

Murali, R.,Ramana, C. V.,Nagarajan, M.

, p. 217 - 218 (2007/10/02)

Syntheses of both forms of cyclopropanated sugars from glycals by (i) Simmons-Smith reaction and (ii) dichlorocarbene addition followed by dehalogenation are described.

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