Cas 867335-89-5,{1-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-2-phenyl-ethyl}-carbamic acid 9<i>H</i>-fluoren-9-ylmethyl ester

867335-89-5

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Basic information

Product Name: {1-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-2-phenyl-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester
Synonyms: {1-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-2-phenyl-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester
CAS NO:867335-89-5
Molecular Formula:
Molecular Weight: 574.676
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: {1-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-2-phenyl-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {1-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-2-phenyl-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester(867335-89-5)
EPA Substance Registry System: {1-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-2-phenyl-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester(867335-89-5)

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: 867335-89-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 867335-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,3,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 867335-89:
(8*8)+(7*6)+(6*7)+(5*3)+(4*3)+(3*5)+(2*8)+(1*9)=215
215 % 10 = 5
So 867335-89-5 is a valid CAS Registry Number.

867335-89-5Upstream product

35661-40-6 N-Fmoc L-Phe

867335-89-5Downstream Products

867335-93-1 (R)-2-Azido-4-methyl-pentanoic acid {(S)-1-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-2-phenyl-ethyl}-amide

867335-89-5Relevant academic research and scientific papers

Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides

Van Maarseveen, Jan H.,Horne, W. Seth,Ghadiri, M. Reza

, p. 4503 - 4506 (2005)

(Chemical Equation Presented) A tandem dimerization-macrocyclization approach using 1,3-dipolar azide-alkyne cycloaddition reactions has been employed in the facile and convergent solution phase syntheses of C2 symmetric cyclic peptide scaffold

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