Cas 1238892-53-9,(3-phenyl-allyl)-carbamic acid di-tert-butyl ester

1238892-53-9

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Basic information

Product Name: (3-phenyl-allyl)-carbamic acid di-tert-butyl ester
Synonyms: (3-phenyl-allyl)-carbamic acid di-tert-butyl ester
CAS NO:1238892-53-9
Molecular Formula:
Molecular Weight: 333.428
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: (3-phenyl-allyl)-carbamic acid di-tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3-phenyl-allyl)-carbamic acid di-tert-butyl ester(1238892-53-9)
EPA Substance Registry System: (3-phenyl-allyl)-carbamic acid di-tert-butyl ester(1238892-53-9)

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: 1238892-53-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1238892-53-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,8,8,9 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1238892-53:
(9*1)+(8*2)+(7*3)+(6*8)+(5*8)+(4*9)+(3*2)+(2*5)+(1*3)=189
189 % 10 = 9
So 1238892-53-9 is a valid CAS Registry Number.

1238892-53-9Upstream product

1238892-53-9Downstream Products

4360-51-4 cinnamylamine

1238892-53-9Relevant academic research and scientific papers

Enantioselective intermolecular bromoesterification of allylic sulfonamides

Zhang, Wei,Liu, Na,Schienebeck, Casi M.,Zhou, Xin,Izhar, Izarin I.,Guzei, Ilia A.,Tang, Weiping

, p. 2652 - 2656 (2013/07/11)

Highly enantioselective intermolecular bromoesterification of alkenes was achieved for the first time. Both C-O and C-Br bonds were introduced enantioselectively in this olefin addition reaction. The sulfonamide NH directing group is important for both th

Iridium-catalyzed allylic substitutions with cyclometalated phosphoramidite complexes bearing a dibenzocyclooctatetraene ligand: Preparation of (π-Allyl)Ir complexes and computational and NMR spectroscopic studies

Raskatov, Jevgenij A.,Jaekel, Mascha,Straub, Bernd F.,Rominger, Frank,Helmchen, Guenter

, p. 14314 - 14328 (2013/01/15)

(π-Allyl)Ir complexes derived from dibenzocyclooctatetraene and phosphoramidites by cyclometalation are effective catalysts for allylic substitution reactions of linear monosubstituted allylic carbonates. These catalysts provide exceptionally high degrees

Heck reaction of arenediazonium salts with N,N-diprotected allylamines. Synthesis of cinnamylamines and indoles

Cacchi, Sandro,Fabrizi, Giancarlo,Goggiamani, Antonella,Sferrazza, Alessio

supporting information; experimental part, p. 1727 - 1730 (2011/05/03)

Novel palladium-catalyzed reactions of arenediazonium tetrafluoroborates with N,N-diprotected allylamines are presented. The reaction of arenediazonium tetrafluoroborates with N,N-(Boc)2 allylamine allows for an easy approach to cinnamylamines whereas using 2-alkynyl-N-(allyl) trifluoroacetanilides and 2-iodo-N-(allyl)trifluoroacetanilide the reaction provides a useful tool for appending indole rings to aniline fragments.

COMPOUNDS FOR THE TREATMENT OF ABNORMAL CELL GROWTH

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Page 101, (2008/06/13)

The invention relates to compounds of the formula (1) and to pharmaceutically acceptable salts, prodrugs and solvates thereof, wherein R1, R2, R3, R4, R5, n, A and B are as defined herein. The inventi

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