Cas 504397-82-4,(1R,2S,3R,4S,5R)-1,2,3,4,5-pentahydroxycyclohexane-1-carboxylic acid

504397-82-4

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Basic information

Product Name: (1R,2S,3R,4S,5R)-1,2,3,4,5-pentahydroxycyclohexane-1-carboxylic acid
Synonyms: (1R,2S,3R,4S,5R)-1,2,3,4,5-pentahydroxycyclohexane-1-carboxylic acid
CAS NO:504397-82-4
Molecular Formula:
Molecular Weight: 208.168
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1R,2S,3R,4S,5R)-1,2,3,4,5-pentahydroxycyclohexane-1-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,3R,4S,5R)-1,2,3,4,5-pentahydroxycyclohexane-1-carboxylic acid(504397-82-4)
EPA Substance Registry System: (1R,2S,3R,4S,5R)-1,2,3,4,5-pentahydroxycyclohexane-1-carboxylic acid(504397-82-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 504397-82-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 504397-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,4,3,9 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 504397-82:
(8*5)+(7*0)+(6*4)+(5*3)+(4*9)+(3*7)+(2*8)+(1*2)=154
154 % 10 = 4
So 504397-82-4 is a valid CAS Registry Number.

504397-82-4Upstream product

504397-81-3 methyl (1R,2S,3R,4S,5R)-1,2,3,4,5-pentahydroxycyclohexane-1-carboxylate

504397-82-4Downstream Products

504397-81-3 methyl (1R,2S,3R,4S,5R)-1,2,3,4,5-pentahydroxycyclohexane-1-carboxylate

504397-82-4Relevant academic research and scientific papers

Synthesis of polyhydroxycyclohexanes and relatives from (-)-quinic acid

Gonzalez, Concepcion,Carballido, Montserrat,Castedo, Luis

, p. 2248 - 2255 (2003)

An efficient and versatile strategy for the synthesis of polyhydroxycyclohexanes and related compounds 3-6 is reported. The successful synthesis of these analogues has been achieved from a common intermediate, quinic acid derived lactone 2, rapidly access

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