Cas 875484-89-2,N-(9-fluorenylmethyloxycarbonyl)-O-[2-acetamido-3,4-di-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-galactopyranosyl]-L-threonine phenacylester

875484-89-2

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Basic information

Product Name: N-(9-fluorenylmethyloxycarbonyl)-O-[2-acetamido-3,4-di-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-galactopyranosyl]-L-threonine phenacylester
Synonyms:
CAS NO:875484-89-2
Molecular Formula:
Molecular Weight: 1077.06
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-(9-fluorenylmethyloxycarbonyl)-O-[2-acetamido-3,4-di-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-galactopyranosyl]-L-threonine phenacylester(CAS DataBase Reference)
NIST Chemistry Reference: N-(9-fluorenylmethyloxycarbonyl)-O-[2-acetamido-3,4-di-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-galactopyranosyl]-L-threonine phenacylester(875484-89-2)
EPA Substance Registry System: N-(9-fluorenylmethyloxycarbonyl)-O-[2-acetamido-3,4-di-O-acetyl-2-deoxy-6-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-galactopyranosyl]-L-threonine phenacylester(875484-89-2)

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: 875484-89-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 875484-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,5,4,8 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 875484-89:
(8*8)+(7*7)+(6*5)+(5*4)+(4*8)+(3*4)+(2*8)+(1*9)=232
232 % 10 = 2
So 875484-89-2 is a valid CAS Registry Number.

875484-89-2Upstream product

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875484-89-2Relevant academic research and scientific papers

Chemical synthesis of analogs of the glycopeptide contulakin-G, an analgetically active conopeptide from Conus geographus

Westerlind, Ulrika,Norberg, Thomas

, p. 9 - 18 (2007/10/03)

Cone snails are marine predators that use immobilizing venoms for catching prey. Chemical analysis of the venoms has revealed a variety of biologically active small and intermediate size peptides rich in post-translational modifications (modified amino ac

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