Cas 201864-27-9,N-((2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-chloro-tetrahydro-pyran-3-yl)-acetamide

201864-27-9

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Basic information

Product Name: N-((2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-chloro-tetrahydro-pyran-3-yl)-acetamide
Synonyms: N-((2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-chloro-tetrahydro-pyran-3-yl)-acetamide
CAS NO:201864-27-9
Molecular Formula:
Molecular Weight: 510.03
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-((2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-chloro-tetrahydro-pyran-3-yl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-chloro-tetrahydro-pyran-3-yl)-acetamide(201864-27-9)
EPA Substance Registry System: N-((2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-chloro-tetrahydro-pyran-3-yl)-acetamide(201864-27-9)

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: 201864-27-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 201864-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,8,6 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 201864-27:
(8*2)+(7*0)+(6*1)+(5*8)+(4*6)+(3*4)+(2*2)+(1*7)=109
109 % 10 = 9
So 201864-27-9 is a valid CAS Registry Number.

201864-27-9Upstream product

201864-27-9Downstream Products

201864-30-4 3-acetamido-2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-glycero-L-gluco-heptonic acid

201864-27-9Relevant academic research and scientific papers

C-glycosides: A stereoselective synthesis of α-C-galactosamines with a glycosyl dianion

Burkhart, Fred,Kessler, Horst

, p. 255 - 256 (1998)

α-C-glycosides of the galactosamine can be obtained from the configurationally stable α-glycosyl dianion which can be prepared by reductive lithiation of the chloride. Different electrophiles react selectively at the anomeric center.

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