Cas 1046152-91-3,3,6-anhydro-4,5,7-tri-O-benzyl-2-deoxy-3-C-(aminomethyl(N-tert-butoxycarbonyl))-D-manno-heptonic acid

1046152-91-3

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Basic information

Product Name: 3,6-anhydro-4,5,7-tri-O-benzyl-2-deoxy-3-C-(aminomethyl(N-tert-butoxycarbonyl))-D-manno-heptonic acid
Synonyms: 3,6-anhydro-4,5,7-tri-O-benzyl-2-deoxy-3-C-(aminomethyl(N-tert-butoxycarbonyl))-D-manno-heptonic acid
CAS NO:1046152-91-3
Molecular Formula:
Molecular Weight: 591.701
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: 3,6-anhydro-4,5,7-tri-O-benzyl-2-deoxy-3-C-(aminomethyl(N-tert-butoxycarbonyl))-D-manno-heptonic acid(CAS DataBase Reference)
NIST Chemistry Reference: 3,6-anhydro-4,5,7-tri-O-benzyl-2-deoxy-3-C-(aminomethyl(N-tert-butoxycarbonyl))-D-manno-heptonic acid(1046152-91-3)
EPA Substance Registry System: 3,6-anhydro-4,5,7-tri-O-benzyl-2-deoxy-3-C-(aminomethyl(N-tert-butoxycarbonyl))-D-manno-heptonic acid(1046152-91-3)

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: 1046152-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1046152-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,1,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1046152-91:
(9*1)+(8*0)+(7*4)+(6*6)+(5*1)+(4*5)+(3*2)+(2*9)+(1*1)=123
123 % 10 = 3
So 1046152-91-3 is a valid CAS Registry Number.

1046152-91-3Upstream product

1046152-92-4 3,6-anhydro-4,5,7-tri-O-benzyl-2-deoxy-3-C-(aminomethyl(N-tert-butoxycarbonyl))-D-manno-heptonic acid lactam

1046152-91-3Downstream Products

1046152-91-3Relevant academic research and scientific papers

Fructose-fused γ-butyrolactones and lactams, synthesis and biological evaluation as GABA receptor ligands

Araujo, Ana C.,Nicotra, Francesco,Costa, Barbara,Giagnoni, Gabriella,Cipolla, Laura

, p. 1840 - 1848 (2008)

We describe the synthesis of sugar-fused β-disubstituted γ-butyrolactones, γ-butyrolactams and a lipophilic β-disubstituted GABA analogue as potential GABA receptor ligands, where the pharmacophore is engineered into the carbohydrate scaffold in the form

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