Cas 82985-17-9,(2R,3S)-3-Benzyloxycarbonylamino-2-hydroxy-5-methyl-hexanoic acid

82985-17-9

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Basic information

Product Name: (2R,3S)-3-Benzyloxycarbonylamino-2-hydroxy-5-methyl-hexanoic acid
Synonyms: (2R,3S)-3-Benzyloxycarbonylamino-2-hydroxy-5-methyl-hexanoic acid
CAS NO:82985-17-9
Molecular Formula:
Molecular Weight: 295.335
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: (2R,3S)-3-Benzyloxycarbonylamino-2-hydroxy-5-methyl-hexanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-3-Benzyloxycarbonylamino-2-hydroxy-5-methyl-hexanoic acid(82985-17-9)
EPA Substance Registry System: (2R,3S)-3-Benzyloxycarbonylamino-2-hydroxy-5-methyl-hexanoic acid(82985-17-9)

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: 82985-17-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 82985-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,8 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82985-17:
(7*8)+(6*2)+(5*9)+(4*8)+(3*5)+(2*1)+(1*7)=169
169 % 10 = 9
So 82985-17-9 is a valid CAS Registry Number.

82985-17-9Upstream product

126535-79-3 (2R,3S)-3-Benzyloxycarbonylamino-2-hydroxy-5-methyl-hexanoic acid methyl ester

82985-17-9Downstream Products

82985-17-9Relevant academic research and scientific papers

Tributyltin Cyanide, a Novel Reagent for the Stereoselective Preparation of 3-Amino-2-hydroxy Acids via Cyanohydrin Intermediates

Herranz, Rosario,Castro-Pichel, Julia,Garcia-Lopez, Teresa

, p. 703 - 706 (1989)

Reaction of tributyltin cyanide with optically active 2-N-benzyloxycarbonylamino aldehydes 1 gives the corresponding O-tributylstannyl cyanohydrins 2 and 3 stereoselectively.Compounds 2 and 3 are transformed in situ into the methyl 3-N-benzyloxycarbonylam

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