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(1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-5-C-hydroxymethyl-1,3,4-cyclohexanetriol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143465-64-9

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143465-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143465-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,4,6 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 143465-64:
(8*1)+(7*4)+(6*3)+(5*4)+(4*6)+(3*5)+(2*6)+(1*4)=129
129 % 10 = 9
So 143465-64-9 is a valid CAS Registry Number.

143465-64-9Relevant academic research and scientific papers

Optimized and Scalable Synthesis of Carba-α-d-Glucosamine

Babczyk, Alexander,Menche, Dirk,Wingen, Lukas M.

, p. 6645 - 6648 (2020/11/16)

An efficient, high-yielding synthesis of carba-α-d-glucosamine is reported. Key features of this optimized route include an innovative protecting group strategy and an unusual, stereoconvergent Ferrier carbocyclization of a hindered substrate. The sequenc

Cyclohexane compounds and their use as antibiotics

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Page/Page column 19, (2012/09/10)

The present invention relates to compounds according to general formula (I), pharmaceutical compositions comprising compounds according to general formula (I) and the use of the compounds for the treatment of a bacterial infection, particularly for use as

CYCLOHEXANE COMPOUNDS AND THEIR USE AS ANTIBIOTICS

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Page/Page column 40, (2012/06/30)

The present invention relates to compounds according to general formula (I), pharmaceutical compositions comprising compounds according to general formula (I) and the use of the compounds for the treatment of a bacterial infection, particularly for use as an antibiotic.

Synthesis of the carbon pseudosugar analog of lipid X

Miyamoto,Baker,Lewis

, p. 3725 - 3728 (2007/10/02)

A carbocyclic analog (2) with a deactivated pseudo-anomeric phosphate of the lipopolysaccharide biosynthetic intermediate Lipid X (1) was prepared in order to better understand the biological behavior of the parent compound. Two related synthetic routes t

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