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78839-75-5

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78839-75-5 Usage

Uses

N-(tert-Butoxycarbonyl)-2-bromoaniline may be used in the synthesis of N-boc-protected o-aryl anilines, which undergoes coupling reaction with bromoacetylenes to form the corresponding arene?ynamides.

General Description

N-(tert-Butoxycarbonyl)-2-bromoaniline, also known as tert-butyl-N-(2-bromophenyl)carbamate, is an N-Boc-protected o-bromoaniline.1 It reacts with ethyl perfluorooctanoate in the presence of tert-butyllithium to form the corresponding 1-hydroxy-1H-perfluorooctyl compound.

Check Digit Verification of cas no

The CAS Registry Mumber 78839-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,3 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78839-75:
(7*7)+(6*8)+(5*8)+(4*3)+(3*9)+(2*7)+(1*5)=195
195 % 10 = 5
So 78839-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H14BrNO2/c1-11(2,3)15-10(14)13-9-7-5-4-6-8(9)12/h4-7H,1-3H3,(H,13,14)

78839-75-5 Well-known Company Product Price

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  • Aldrich

  • (531316)  N-(tert-Butoxycarbonyl)-2-bromoaniline  97%

  • 78839-75-5

  • 531316-10G

  • 2,558.79CNY

  • Detail

78839-75-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(2-bromophenyl)carbamate

1.2 Other means of identification

Product number -
Other names N-(tert-Butoxycarbonyl)-2-bromoaniline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:78839-75-5 SDS

78839-75-5Relevant articles and documents

A robust pure hydrocarbon derivative based on the (2,1-b)-indenofluorenyl core with high triplet energy level

Poriel, Cyril,Metivier, Remi,Rault-Berthelot, Joelle,Thirion, Damien,Barriere, Frederic,Jeannin, Olivier

, p. 11703 - 11705 (2011)

A unique (2,1-b)-indenofluorenyl core flanked with two spirofluorene units, possessing a high triplet energy value and excellent thermal/morphological stability, is reported.

A Rh(II)- or Ag(I)-Catalyzed Formal C-O Bond Insertion of Cyclic Hemiaminal with Aryl Diazoacetate

Xu, Cong,Liu, Xiangrong,Xie, Xiongda,Deng, Lin,Xu, Xinfang,Chan, Albert S. C.,Hu, Wenhao

supporting information, p. 1957 - 1962 (2021/09/22)

A mild and facile synthetic method via convergent assembly of two reactive intermediates generated in situ has been developed. This method provides an efficient way to construct six- and sevenmembered N-heterocycles containing a biaryl linkage. This react

Domino Pd0-Catalyzed C(sp3)–H Arylation/Electrocyclic Reactions via Benzazetidine Intermediates

Rocaboy, Ronan,Dailler, David,Zellweger, Florian,Neuburger, Markus,Salomé, Christophe,Clot, Eric,Baudoin, Olivier

, p. 12131 - 12135 (2018/09/11)

The Pd0-catalyzed C(sp3)-H arylation of 2-bromo-N-methylanilides leads to unstable benzazetidine intermediates that rearrange to benzoxazines through 4π electrocyclic ring-opening and 6π electrocyclization. The introduction of a bulky, non-activatable amide group on the nitrogen atom was key to favor the challenging reductive elimination step and disfavor undesired reaction pathways.

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