Cas 443770-00-1,5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoic acid [4-(4-amino-benzylcarbamoyl)-butyl]-amide

443770-00-1

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Basic information

Product Name: 5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoic acid [4-(4-amino-benzylcarbamoyl)-butyl]-amide
Synonyms: 5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoic acid [4-(4-amino-benzylcarbamoyl)-butyl]-amide
CAS NO:443770-00-1
Molecular Formula:
Molecular Weight: 447.602
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: 5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoic acid [4-(4-amino-benzylcarbamoyl)-butyl]-amide(CAS DataBase Reference)
NIST Chemistry Reference: 5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoic acid [4-(4-amino-benzylcarbamoyl)-butyl]-amide(443770-00-1)
EPA Substance Registry System: 5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoic acid [4-(4-amino-benzylcarbamoyl)-butyl]-amide(443770-00-1)

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: 443770-00-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 443770-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,7,7 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 443770-00:
(8*4)+(7*4)+(6*3)+(5*7)+(4*7)+(3*0)+(2*0)+(1*0)=141
141 % 10 = 1
So 443770-00-1 is a valid CAS Registry Number.

443770-00-1Upstream product

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443770-00-1Relevant academic research and scientific papers

Design and synthesis of biotin chain-terminated glycopolymers for surface glycoengineering

Sun, Xue-Long,Faucher, Keith M.,Houston, Michelle,Grande, Daniel,Chaikof, Elliot L.

, p. 7258 - 7259 (2002)

Biotin chain-terminated glycopolymers were generated by cyanoxyl-mediated free-radical polymerization using a biotin-derivatized arylamine initiator with high conversion (75%) and low polydispersity (1.30). Streptavidin-biotinylated glycopolymer binding w

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