Cas 917610-46-9,[5-<i>tert</i>-butoxycarbonylamino-5-(2-dodecanoyl-phenylcarbamoyl)-pentyl]-carbamic acid benzyl ester

917610-46-9

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Basic information

Product Name: [5-tert-butoxycarbonylamino-5-(2-dodecanoyl-phenylcarbamoyl)-pentyl]-carbamic acid benzyl ester
Synonyms: [5-tert-butoxycarbonylamino-5-(2-dodecanoyl-phenylcarbamoyl)-pentyl]-carbamic acid benzyl ester
CAS NO:917610-46-9
Molecular Formula:
Molecular Weight: 637.86
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: [5-tert-butoxycarbonylamino-5-(2-dodecanoyl-phenylcarbamoyl)-pentyl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [5-tert-butoxycarbonylamino-5-(2-dodecanoyl-phenylcarbamoyl)-pentyl]-carbamic acid benzyl ester(917610-46-9)
EPA Substance Registry System: [5-tert-butoxycarbonylamino-5-(2-dodecanoyl-phenylcarbamoyl)-pentyl]-carbamic acid benzyl ester(917610-46-9)

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: 917610-46-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 917610-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,6,1 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 917610-46:
(8*9)+(7*1)+(6*7)+(5*6)+(4*1)+(3*0)+(2*4)+(1*6)=169
169 % 10 = 9
So 917610-46-9 is a valid CAS Registry Number.

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917610-46-9Relevant academic research and scientific papers

Rapid approach to 3,5-disubstituted 1,4-benzodiazepines via the photo-fries rearrangement of anilides

Ferrini, Serena,Ponticelli, Fabio,Taddei, Maurizio

, p. 9217 - 9220 (2007/10/03)

(Chemical Equation Presented) Different anilides derived from carboxylic acids and substituted anilines have been submitted to the photochemically induced Fries rearrangement giving the corresponding o-amino phenones under conditions that are compatible w

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