Cas 98383-36-9,methyl 3-{[(2-chloroethyl)(nitroso)carbamoyl]amino}-2,3,6-trideoxy-alpha-L-arabino-hexopyranoside

98383-36-9

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Basic information

Product Name: methyl 3-{[(2-chloroethyl)(nitroso)carbamoyl]amino}-2,3,6-trideoxy-alpha-L-arabino-hexopyranoside
Synonyms:
CAS NO:98383-36-9
Molecular Formula: C₁₀H₁₈ClN₃O₅
Molecular Weight: 295.72
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: 1.49g/cm³
Refractive Index: 1.578
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: methyl 3-{[(2-chloroethyl)(nitroso)carbamoyl]amino}-2,3,6-trideoxy-alpha-L-arabino-hexopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3-{[(2-chloroethyl)(nitroso)carbamoyl]amino}-2,3,6-trideoxy-alpha-L-arabino-hexopyranoside(98383-36-9)
EPA Substance Registry System: methyl 3-{[(2-chloroethyl)(nitroso)carbamoyl]amino}-2,3,6-trideoxy-alpha-L-arabino-hexopyranoside(98383-36-9)

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: 98383-36-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98383-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,8 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 98383-36:
(7*9)+(6*8)+(5*3)+(4*8)+(3*3)+(2*3)+(1*6)=179
179 % 10 = 9
So 98383-36-9 is a valid CAS Registry Number.

98383-36-9Upstream product

54623-23-3 methyl-3-amino-2,3,6-tridesoxy-α-L-arabino-hexopyranoside

98383-36-9Downstream Products

98383-36-9Relevant academic research and scientific papers

Rationale for the synthesis and preliminary biological evaluation of highly active new antitumor nitrosoureido sugars

Roger,Monneret,Fournier,Choay,Gagnet,Gosse,Letourneux,Atassi,Gouyette

, p. 16 - 23 (2007/10/02)

Various new nitrosoureido derivatives of di- or trideoxy sugars were synthesized. The influence of the hydroxyl substutition pattern, the configuration at the anomeric center, and the absolute configuration of the sugar moiety on the antitumor activity of

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