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Benzoic acid (1S,2S,6R)-2-bromo-6-hydroxy-4-methoxycarbonyl-cyclohex-3-enyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

179738-33-1

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179738-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 179738-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,7,3 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 179738-33:
(8*1)+(7*7)+(6*9)+(5*7)+(4*3)+(3*8)+(2*3)+(1*3)=191
191 % 10 = 1
So 179738-33-1 is a valid CAS Registry Number.

179738-33-1Upstream product

179738-33-1Relevant academic research and scientific papers

Synthesis of (-)-3(R)-amino-4(R),5(R)-dihydroxy-1-cyclohexene-1-carboxylic acid: The 3(R)-amino analogue of (-)-shikimic acid

Brettle, Roger,Cross, Richard,Frederickson, Martyn,Haslam, Edwin,Davies, Gareth M.

, p. 291 - 294 (1996)

(-)-3(R)-Amino-4(R),5(R)-dihydroxy-1-cyclohexene-1-carboxylic acid (the 3(R)-amino analogue of (-)-shikimic acid) has been synthesised from (-)-shikimic acid in seven steps. Copyright

Synthesis and evaluation of 2,5-dihydrochorismate analogues as inhibitors of the chorismate-utilising enzymes

Payne, Richard J.,Bulloch, Esther M. M.,Toscano, Miguel M.,Jones, Michelle A.,Kerbarh, Olivier,Abell, Chris

scheme or table, p. 2421 - 2429 (2009/09/26)

A library of 2,5-dihydrochorismate analogues were designed as inhibitors of the chorismate-utilising enzymes including anthranilate synthase, isochorismate synthase, salicylate synthase and 4-amino-4-deoxychorismate synthase. The inhibitors were synthesis

Synthesis of (3R)- and (3S)-fluoro-(4R,5R)-dihydroxy-1-cyclohexene-1- carboxylic acids: The (3R)- and (3S)-fluoro analogues of (-)-shikimic acid

Brettle,Cross,Frederickson,Haslam,MacBeath,Davies

, p. 1275 - 1278 (2007/10/03)

(3R)-and (3S)-Fluoro-(4R,5R)-dihydroxy-1-cyclohexene-1-carboxylic acids (the (3R)- and (3S)-fluoro analogues of (-)-shikimic acid) have been synthesised from (-)-shikimic acid via an intermediate epoxide (a fungal metabolite from Chalara microspora) that

The shikimate pathway. Part 8. Synthesis of (-)-3(R)-amino- 4(R),5(R)-dihydroxy-1-cyclohexene-1-carboxylic acid: The 3(R)- amino analogue of (-)-shikimic acid

Adams,Bailey,Brettle,Cross,Frederickson,Haslam,MacBeath,Davies

, p. 8565 - 8580 (2007/10/03)

The first successful method for the introduction of nitrogenous functionality at C-3 of the shikimate nucleus has been developed and has allowed the synthesis of (-)-3(R)-amino-4(R),5(R)- dihydroxy-1-cyclohexene-1-carboxylic acid [the 3(R)-amino analogue of (-)-shikimic acid] in seven steps from the parent acid.

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