Cas 1151801-27-2,N-(β-L-arabinofuranos-1-yl)-N-(2-nitrobenzenesulfonyl)-L-phenylalanine

1151801-27-2

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Basic information

Product Name: N-(β-L-arabinofuranos-1-yl)-N-(2-nitrobenzenesulfonyl)-L-phenylalanine
Synonyms: N-(β-L-arabinofuranos-1-yl)-N-(2-nitrobenzenesulfonyl)-L-phenylalanine
CAS NO:1151801-27-2
Molecular Formula:
Molecular Weight: 482.468
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: N-(β-L-arabinofuranos-1-yl)-N-(2-nitrobenzenesulfonyl)-L-phenylalanine(CAS DataBase Reference)
NIST Chemistry Reference: N-(β-L-arabinofuranos-1-yl)-N-(2-nitrobenzenesulfonyl)-L-phenylalanine(1151801-27-2)
EPA Substance Registry System: N-(β-L-arabinofuranos-1-yl)-N-(2-nitrobenzenesulfonyl)-L-phenylalanine(1151801-27-2)

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: 1151801-27-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1151801-27-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,1,8,0 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1151801-27:
(9*1)+(8*1)+(7*5)+(6*1)+(5*8)+(4*0)+(3*1)+(2*2)+(1*7)=112
112 % 10 = 2
So 1151801-27-2 is a valid CAS Registry Number.

1151801-27-2Upstream product

1151800-98-4 N-(2,3,5-tri-O-acetyl-β-L-arabinofuranos-1-yl)-N-(2-nitrobenzenesulfonyl)-L-phenylalanine

1151801-27-2Downstream Products

1151801-27-2Relevant academic research and scientific papers

Stereoselective synthesis of novel N-(α-l-arabinofuranos-1-yl)-l-amino acids

Zhao, Ming,Wang, Yuji,Huo, Caixia,Li, Chunyu,Zhang, Xiaoyi,Peng, Li,Peng, Shiqi

experimental part, p. 247 - 258 (2009/06/28)

In lead detoxification, the α-anomer of N-glycocyl-l-amino acid is more potent than its β-anomer. Here a six-step-reaction route for stereoselectively preparing N-(α-l-arabinose-1-yl)-l-amino acids is reported. Treating l-arabinose with acetic anhydride a

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