Cas 1201815-28-2,(1S,2R,4R,5S)-2-amino-4,5-dihydroxycyclohexanecarboxylic acid hydrochloride

1201815-28-2

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Basic information

Product Name: (1S,2R,4R,5S)-2-amino-4,5-dihydroxycyclohexanecarboxylic acid hydrochloride
Synonyms: (1S,2R,4R,5S)-2-amino-4,5-dihydroxycyclohexanecarboxylic acid hydrochloride
CAS NO:1201815-28-2
Molecular Formula:
Molecular Weight: 211.645
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: (1S,2R,4R,5S)-2-amino-4,5-dihydroxycyclohexanecarboxylic acid hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,4R,5S)-2-amino-4,5-dihydroxycyclohexanecarboxylic acid hydrochloride(1201815-28-2)
EPA Substance Registry System: (1S,2R,4R,5S)-2-amino-4,5-dihydroxycyclohexanecarboxylic acid hydrochloride(1201815-28-2)

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: 1201815-28-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1201815-28-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,8,1 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1201815-28:
(9*1)+(8*2)+(7*0)+(6*1)+(5*8)+(4*1)+(3*5)+(2*2)+(1*8)=102
102 % 10 = 2
So 1201815-28-2 is a valid CAS Registry Number.

1201815-28-2Upstream product

1201815-20-4 ethyl (1S,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate

1201815-28-2Downstream Products

1201815-28-2Relevant academic research and scientific papers

Efficient synthesis of 3,4- and 4,5-dihydroxy-2-amino-cyclohexanecarboxylic acid enantiomers

Benedek, Gabriella,Palko, Marta,Weber, Edit,Martinek, Tamas A.,Forro, Eniko,Fueloep, Ferenc

experimental part, p. 2220 - 2225 (2010/03/03)

An efficient method for the synthesis of (1S,2R,4R,5S)- and (1R,2R,4R,5S)-2-amino-4,5-dihydroxycyclohexanecarboxylic acids (-)-6 and (-)-9 and (1R,2R,3S,4R)- and (1S,2R,3S,4R)-2-amino-3,4-dihydroxycyclohexanecarboxylic acids (-)-15 and (-)-18 was develope

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