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6-trifluoroacetamidohexyl O-[methyl (5-amino-5-N,4-O-carbonyl-7,8,9-tri-O-chloroacetyl-3,5-dideoxy-D-glycero-α-D-galactonon-2-ulopyranoside)onate]-(2->3)-O-(2,6-di-O-benzyl-α-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1235555-41-5

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1235555-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1235555-41-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,5,5 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1235555-41:
(9*1)+(8*2)+(7*3)+(6*5)+(5*5)+(4*5)+(3*5)+(2*4)+(1*1)=145
145 % 10 = 5
So 1235555-41-5 is a valid CAS Registry Number.

1235555-41-5Downstream Products

1235555-41-5Relevant academic research and scientific papers

5- N,4- O -carbonyl-7,8,9-tri- O -chloroacetyl-protected sialyl donor for the stereoselective synthesis of α-(2→9)-tetrasialic acid

Lin, Chang-Ching,Lin, Nai-Pin,Sahabuddin, L. Sk,Reddy, Vijaya Raghava,Huang, Li-De,Hwang, Kuo Chu,Lin, Chun-Cheng

, p. 4921 - 4928 (2010)

(Figure presented) An efficient stereoselective synthesis of α-(2→9)-tetrasialic acid was achieved using tri-O-chloroacetyl- derivatized sialyl donor and a triol sialyl acceptor. Both the acceptor and the donor were also protected with a cyclic 5-N-4-O-carbonyl protecting group. The donor is highly reactive and enabled α-selective sialylation with various primary, secondary, and tertiary acceptors under in situ activation conditions (NIS/TfOH, -78 °C, acetonitrile/dichloromethane). The trans-fused oxazolidinone ring and O-chloroacetyl protecting groups were easily removed under mild reaction conditions to provide the fully deprotected α(2→9)-tetrasialic acid.

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