Cas 1185885-15-7,5-(N-tert-butoxycarbonyl-N-methylaminomethyl)-3H-1,2,3-triazole-4-carboxylic acid benzyl ester

1185885-15-7

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Basic information

Product Name: 5-(N-tert-butoxycarbonyl-N-methylaminomethyl)-3H-1,2,3-triazole-4-carboxylic acid benzyl ester
Synonyms: 5-(N-tert-butoxycarbonyl-N-methylaminomethyl)-3H-1,2,3-triazole-4-carboxylic acid benzyl ester
CAS NO:1185885-15-7
Molecular Formula:
Molecular Weight: 346.386
EINECS: N/A
Product Categories: N/A
Mol File: 1185885-15-7.mol
Article Data: 1

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-(N-tert-butoxycarbonyl-N-methylaminomethyl)-3H-1,2,3-triazole-4-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-(N-tert-butoxycarbonyl-N-methylaminomethyl)-3H-1,2,3-triazole-4-carboxylic acid benzyl ester(1185885-15-7)
EPA Substance Registry System: 5-(N-tert-butoxycarbonyl-N-methylaminomethyl)-3H-1,2,3-triazole-4-carboxylic acid benzyl ester(1185885-15-7)

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: 1185885-15-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1185885-15-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,5,8,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1185885-15:
(9*1)+(8*1)+(7*8)+(6*5)+(5*8)+(4*8)+(3*5)+(2*1)+(1*5)=197
197 % 10 = 7
So 1185885-15-7 is a valid CAS Registry Number.

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1185885-15-7Relevant articles and documents

Novel triazolopeptides: chirospecific synthesis and conformational studies of proline derived analogs

Paul, Andreas,Einsiedel, Juergen,Waibel, Reiner,Heinemann, Frank W.,Meyer, Karsten,Gmeiner, Peter

, p. 6156 - 6168 (2011/03/21)

Replacing the backbone amide function by a heterocyclic bioisostere, [3+2] azide-alkyne cycloaddition has been applied for the construction of biologically relevant peptidomimetics. Starting from aminoalkynoates, triazole formation was accomplished by add

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