Cas 506410-45-3,(R)-4-benzyl-3-[(S)-3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)butyryl]oxazolidin-2-one

506410-45-3

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Basic information

Product Name: (R)-4-benzyl-3-[(S)-3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)butyryl]oxazolidin-2-one
Synonyms: (R)-4-benzyl-3-[(S)-3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)butyryl]oxazolidin-2-one
CAS NO:506410-45-3
Molecular Formula:
Molecular Weight: 783.962
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)-4-benzyl-3-[(S)-3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)butyryl]oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (R)-4-benzyl-3-[(S)-3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)butyryl]oxazolidin-2-one(506410-45-3)
EPA Substance Registry System: (R)-4-benzyl-3-[(S)-3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)butyryl]oxazolidin-2-one(506410-45-3)

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: 506410-45-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 506410-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,6,4,1 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 506410-45:
(8*5)+(7*0)+(6*6)+(5*4)+(4*1)+(3*0)+(2*4)+(1*5)=113
113 % 10 = 3
So 506410-45-3 is a valid CAS Registry Number.

506410-45-3Upstream product

506410-45-3Downstream Products

506410-45-3Relevant academic research and scientific papers

Synthesis of a C-glycoside analogue of β-D-galactosylthreonine

Gustafsson, Tomas,Saxin, Maria,Kihlberg, Jan

, p. 2506 - 2509 (2003)

A C-linked analogue of β-D-galactosylthreonine has been prepared from 2,3,4,6-tetra-O-benzyl-D-galactopyranolactone (1) in 14 steps. Three stereogenic centers were created during the synthesis, with the anomeric center of the C-glycoside being generated f

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