Cas 1009643-30-4,N-[3,4,6-tri-O-acetyl-2-N-(allyloxycarbonyl)-2-amino-2-deoxy-β-D-glucopyranosyl]-carbamoyl-L-tert-leucinyl-benzylamide

1009643-30-4

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Basic information

Product Name: N-[3,4,6-tri-O-acetyl-2-N-(allyloxycarbonyl)-2-amino-2-deoxy-β-D-glucopyranosyl]-carbamoyl-L-tert-leucinyl-benzylamide
Synonyms: N-[3,4,6-tri-O-acetyl-2-N-(allyloxycarbonyl)-2-amino-2-deoxy-β-D-glucopyranosyl]-carbamoyl-L-tert-leucinyl-benzylamide
CAS NO:1009643-30-4
Molecular Formula:
Molecular Weight: 634.684
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-[3,4,6-tri-O-acetyl-2-N-(allyloxycarbonyl)-2-amino-2-deoxy-β-D-glucopyranosyl]-carbamoyl-L-tert-leucinyl-benzylamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[3,4,6-tri-O-acetyl-2-N-(allyloxycarbonyl)-2-amino-2-deoxy-β-D-glucopyranosyl]-carbamoyl-L-tert-leucinyl-benzylamide(1009643-30-4)
EPA Substance Registry System: N-[3,4,6-tri-O-acetyl-2-N-(allyloxycarbonyl)-2-amino-2-deoxy-β-D-glucopyranosyl]-carbamoyl-L-tert-leucinyl-benzylamide(1009643-30-4)

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: 1009643-30-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1009643-30-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,9,6,4 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1009643-30:
(9*1)+(8*0)+(7*0)+(6*9)+(5*6)+(4*4)+(3*3)+(2*3)+(1*0)=124
124 % 10 = 4
So 1009643-30-4 is a valid CAS Registry Number.

1009643-30-4Upstream product

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1009643-30-4Relevant academic research and scientific papers

Enantioselective organocatalysis of Strecker and Mannich reactions based on carbohydrates

Becker, Christian,Hoben, Christine,Kunz, Horst

, p. 417 - 424 (2008/02/07)

Efficient organocatalysts for enantioselective Strecker and Mannich reactions were constructed from glucosamine as a readily accessible chiral scaffold. A variety of aromatic aldimines were subjected to hydrocyanation with good to excellent yield (72-98%)

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