Cas 157029-53-3,[(R)-1-((2S,3S,4R,5S)-4-Benzyloxy-3-hydroxy-5-methoxy-tetrahydro-furan-2-yl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester

157029-53-3

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Basic information

Product Name: [(R)-1-((2S,3S,4R,5S)-4-Benzyloxy-3-hydroxy-5-methoxy-tetrahydro-furan-2-yl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester
Synonyms:
CAS NO:157029-53-3
Molecular Formula:
Molecular Weight: 383.442
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: [(R)-1-((2S,3S,4R,5S)-4-Benzyloxy-3-hydroxy-5-methoxy-tetrahydro-furan-2-yl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(R)-1-((2S,3S,4R,5S)-4-Benzyloxy-3-hydroxy-5-methoxy-tetrahydro-furan-2-yl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester(157029-53-3)
EPA Substance Registry System: [(R)-1-((2S,3S,4R,5S)-4-Benzyloxy-3-hydroxy-5-methoxy-tetrahydro-furan-2-yl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester(157029-53-3)

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: 157029-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 157029-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,0,2 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 157029-53:
(8*1)+(7*5)+(6*7)+(5*0)+(4*2)+(3*9)+(2*5)+(1*3)=133
133 % 10 = 3
So 157029-53-3 is a valid CAS Registry Number.

157029-53-3Upstream product

157029-53-3Downstream Products

107537-94-0 (+)-Galactostatin

157029-53-3Relevant academic research and scientific papers

Synthesis of (+)-Galactostatin and (+)-1-Deoxygalactostatin utilizing L-Quebrachitol as a Chiral Building Block

Chida, Noritaka,Tanikawa, Tetsuya,Tobe, Takahiko,Ogawa, Seiichiro

, p. 1247 - 1248 (2007/10/02)

The stereoselective conversion of the naturally occurring optically active cyclitol, L-quebrachitol 1, into galactosidase inhibitors, (+)-galactostatin 2 and (+)-1-deoxygalactostatin 3 is described; the key steps in this synthesis are (i) stereoselective

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