Cas 1248592-64-4,N-palmitoyl-S-[(2R)-2,3-bis(palmitoyloxy)propyl]-(R)-cysteinyl-(O-tert-butyl)-(S)-serinyl-NH(CH2CH2O)2CH2CO2H

1248592-64-4

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Basic information

Product Name: N-palmitoyl-S-[(2R)-2,3-bis(palmitoyloxy)propyl]-(R)-cysteinyl-(O-tert-butyl)-(S)-serinyl-NH(CH₂CH₂O)2CH₂CO₂H
Synonyms: N-palmitoyl-S-[(2R)-2,3-bis(palmitoyloxy)propyl]-(R)-cysteinyl-(O-tert-butyl)-(S)-serinyl-NH(CH₂CH₂O)2CH₂CO₂H
CAS NO:1248592-64-4
Molecular Formula:
Molecular Weight: 1198.82
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-palmitoyl-S-[(2R)-2,3-bis(palmitoyloxy)propyl]-(R)-cysteinyl-(O-tert-butyl)-(S)-serinyl-NH(CH₂CH₂O)2CH₂CO₂H(CAS DataBase Reference)
NIST Chemistry Reference: N-palmitoyl-S-[(2R)-2,3-bis(palmitoyloxy)propyl]-(R)-cysteinyl-(O-tert-butyl)-(S)-serinyl-NH(CH₂CH₂O)2CH₂CO₂H(1248592-64-4)
EPA Substance Registry System: N-palmitoyl-S-[(2R)-2,3-bis(palmitoyloxy)propyl]-(R)-cysteinyl-(O-tert-butyl)-(S)-serinyl-NH(CH₂CH₂O)2CH₂CO₂H(1248592-64-4)

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: 1248592-64-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1248592-64-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,8,5,9 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1248592-64:
(9*1)+(8*2)+(7*4)+(6*8)+(5*5)+(4*9)+(3*2)+(2*6)+(1*4)=184
184 % 10 = 4
So 1248592-64-4 is a valid CAS Registry Number.

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1248592-64-4Relevant academic research and scientific papers

Synthesis of MUC1-lipopeptide chimeras

Wilkinson, Brendan L.,Malins, Lara R.,Chun, Candy K. Y.,Payne, Richard J.

, p. 6249 - 6251 (2010)

An efficient method for the convergent assembly of MUC1-lipopeptide vaccine candidates is described. Chimeras consisting of MUC1 glycopeptides (bearing multiple copies of the TN and T tumour-associated carbohydrate antigens) tethered to the lipopeptide immunoadjuvant Pam3CysSer were synthesised in high yields using a fragment-based condensation strategy.

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