Cas 867335-82-8,{(S)-5-((R)-2-Azido-4-methyl-pentanoylamino)-5-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-pentyl}-carbamic acid tert-butyl ester

867335-82-8

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Basic information

Product Name: {(S)-5-((R)-2-Azido-4-methyl-pentanoylamino)-5-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-pentyl}-carbamic acid tert-butyl ester
Synonyms: {(S)-5-((R)-2-Azido-4-methyl-pentanoylamino)-5-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-pentyl}-carbamic acid tert-butyl ester
CAS NO:867335-82-8
Molecular Formula:
Molecular Weight: 572.705
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: {(S)-5-((R)-2-Azido-4-methyl-pentanoylamino)-5-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-pentyl}-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(S)-5-((R)-2-Azido-4-methyl-pentanoylamino)-5-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-pentyl}-carbamic acid tert-butyl ester(867335-82-8)
EPA Substance Registry System: {(S)-5-((R)-2-Azido-4-methyl-pentanoylamino)-5-[(2,4-dimethoxy-benzyl)-prop-2-ynyl-carbamoyl]-pentyl}-carbamic acid tert-butyl ester(867335-82-8)

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: 867335-82-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 867335-82-8 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 867335-82:
(8*8)+(7*6)+(6*7)+(5*3)+(4*3)+(3*5)+(2*8)+(1*2)=208
208 % 10 = 8
So 867335-82-8 is a valid CAS Registry Number.

867335-82-8Upstream product

867335-82-8Downstream Products

867335-83-9 {4-[16-(4-tert-butoxycarbonylamino-butyl)-7,18-bis-(2,4-dimethoxy-benzyl)-2,13-diisobutyl-3,6,14,17-tetraoxo-1,4,7,10,11,12,15,18,21,22-decaaza-tricyclo[18.2.1.1^9,12]tetracosa-9⁽²⁴⁾,10,20⁽²³⁾,21-tetraen-5-yl]-butyl}-carbamic acid tert-butyl ester

867335-82-8Relevant 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 (2007/10/03)

(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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