Cas 852325-27-0,N-allyloxycarbonyl-L-methionyl-L-tyrosyl-L-(3-bromo-alanine) methyl ester

852325-27-0

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Basic information

Product Name: N-allyloxycarbonyl-L-methionyl-L-tyrosyl-L-(3-bromo-alanine) methyl ester
Synonyms: N-allyloxycarbonyl-L-methionyl-L-tyrosyl-L-(3-bromo-alanine) methyl ester
CAS NO:852325-27-0
Molecular Formula:
Molecular Weight: 560.466
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-allyloxycarbonyl-L-methionyl-L-tyrosyl-L-(3-bromo-alanine) methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-allyloxycarbonyl-L-methionyl-L-tyrosyl-L-(3-bromo-alanine) methyl ester(852325-27-0)
EPA Substance Registry System: N-allyloxycarbonyl-L-methionyl-L-tyrosyl-L-(3-bromo-alanine) methyl ester(852325-27-0)

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: 852325-27-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 852325-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,3,2 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 852325-27:
(8*8)+(7*5)+(6*2)+(5*3)+(4*2)+(3*5)+(2*2)+(1*7)=160
160 % 10 = 0
So 852325-27-0 is a valid CAS Registry Number.

852325-27-0Upstream product

852325-27-0Downstream Products

852325-27-0Relevant academic research and scientific papers

Reversed approach to S-farnesylation and S-palmitoylation: Application to an efficient synthesis of the C-terminus of lipidated human N-Ras hexapeptide

Pachamuthu, Kandasamy,Zhu, Xiangming,Schmidt, Richard R.

, p. 3720 - 3723 (2005)

(Chemical Equation Presented) A general reversed approach is described to synthesize S-palmitoylated and S-farnesylated peptides via SN2 displacement of bromide by reaction of a thiol group containing lipid as nucleophile with bromoalanine-cont

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