Cas 1353020-69-5,(-)-(1'R,2'R,3'R,5'S)-(2,6,6-trimethylbicyclo[3.1.1]hept-3-yl) 6-O-acetyl-2-benzamido-2,3,4-trideoxy-α-D-erythro-hex-3-enopyranoside

1353020-69-5

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Basic information

Product Name: (-)-(1'R,2'R,3'R,5'S)-(2,6,6-trimethylbicyclo[3.1.1]hept-3-yl) 6-O-acetyl-2-benzamido-2,3,4-trideoxy-α-D-erythro-hex-3-enopyranoside
Synonyms:
CAS NO:1353020-69-5
Molecular Formula:
Molecular Weight: 427.541
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: (-)-(1'R,2'R,3'R,5'S)-(2,6,6-trimethylbicyclo[3.1.1]hept-3-yl) 6-O-acetyl-2-benzamido-2,3,4-trideoxy-α-D-erythro-hex-3-enopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(1'R,2'R,3'R,5'S)-(2,6,6-trimethylbicyclo[3.1.1]hept-3-yl) 6-O-acetyl-2-benzamido-2,3,4-trideoxy-α-D-erythro-hex-3-enopyranoside(1353020-69-5)
EPA Substance Registry System: (-)-(1'R,2'R,3'R,5'S)-(2,6,6-trimethylbicyclo[3.1.1]hept-3-yl) 6-O-acetyl-2-benzamido-2,3,4-trideoxy-α-D-erythro-hex-3-enopyranoside(1353020-69-5)

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: 1353020-69-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1353020-69-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,0,2 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1353020-69:
(9*1)+(8*3)+(7*5)+(6*3)+(5*0)+(4*2)+(3*0)+(2*6)+(1*9)=115
115 % 10 = 5
So 1353020-69-5 is a valid CAS Registry Number.

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1353020-69-5Relevant academic research and scientific papers

Glucosaminides proceeding from levoglycosenone

Faizullina, L. Kh.,Iskakova,Salikhov, Sh. M.,Safarov,Valeev

, p. 1750 - 1754 (2011)

The possibility was studied of using levoglycosenone in the synthesis of N-(glucosen-2-yl) aminides. New glucosaminides were obtained containing the residues of L-a, isopinocampheol, borneol, and (-)-(1S,2R,3S,7S,8R)-4,4- dimethyl-3-nitro-9,11-dioxatricyc

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