Cas 133798-07-9,methyl 2-(4'6'-O-isopropylidene-2',3'-epoxy-β-D-mannopyranosyl)-2-benzamido-(2R)-propionate

133798-07-9

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Basic information

Product Name: methyl 2-(4'6'-O-isopropylidene-2',3'-epoxy-β-D-mannopyranosyl)-2-benzamido-(2R)-propionate
Synonyms: methyl 2-(4'6'-O-isopropylidene-2',3'-epoxy-β-D-mannopyranosyl)-2-benzamido-(2R)-propionate
CAS NO:133798-07-9
Molecular Formula:
Molecular Weight: 391.421
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: methyl 2-(4'6'-O-isopropylidene-2',3'-epoxy-β-D-mannopyranosyl)-2-benzamido-(2R)-propionate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-(4'6'-O-isopropylidene-2',3'-epoxy-β-D-mannopyranosyl)-2-benzamido-(2R)-propionate(133798-07-9)
EPA Substance Registry System: methyl 2-(4'6'-O-isopropylidene-2',3'-epoxy-β-D-mannopyranosyl)-2-benzamido-(2R)-propionate(133798-07-9)

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: 133798-07-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133798-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,9 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133798-07:
(8*1)+(7*3)+(6*3)+(5*7)+(4*9)+(3*8)+(2*0)+(1*7)=149
149 % 10 = 9
So 133798-07-9 is a valid CAS Registry Number.

133798-07-9Upstream product

133798-07-9Downstream Products

133779-01-8 2-(β-D-altropyranosyl)-2-benzamido-(2R)-propionic acid 1',2'-lactone

133798-07-9Relevant academic research and scientific papers

Stereoselective Synthesis of C-Glycosyl α-Amino Acids

Colombo, Lino,Casiraghi, Giovanni,Pittalis, Antonello,Rassu, Gloria

, p. 3897 - 3900 (2007/10/02)

β-D-C-Allosyl-(R)-alanine 12 and β-D-C-altrosyl-(R)-alanine lactone 15 were synthesized from the common intermediate 7 in just a few steps.The β-C-glycosyloxazolone 7 was obtained in two steps from the protected D-glucal 4 by a sequential coupling with N-benzoylalanine followed by a Claisen rearrangement.

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