Passa al contenuto
Merck
Tutte le immagini(2)

Documenti

180025

Sigma-Aldrich

3-Bromoaniline

98%

Sinonimo/i:

(3-Bromophenyl)amine, (m-Bromophenyl)amine, 1-Amino-3-bromobenzene, 3-Amino-1-bromobenzene, 3-Bromobenzenamine, m-Aminobromobenzene, m-Bromoaniline

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(2)

About This Item

Formula condensata:
BrC6H4NH2
Numero CAS:
591-19-5
Peso molecolare:
172.02
Beilstein:
742028
Numero CE:
209-704-4
Numero MDL:
MFCD00007757
Codice UNSPSC:
12352100
ID PubChem:
24850844
NACRES:
NA.22

Saggio

98%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.625 (lit.)

P. eboll.

251 °C (lit.)

Punto di fusione

15-18 °C (lit.)

Densità

1.58 g/mL at 25 °C (lit.)

Stringa SMILE

Nc1cccc(Br)c1

InChI

1S/C6H6BrN/c7-5-2-1-3-6(8)4-5/h1-4H,8H2
DHYHYLGCQVVLOQ-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Descrizione generale

The in vitro nephrotoxic potential of 3-bromoaniline was studied.

Applicazioni

3-Bromoaniline was used in the synthesis of amino substituted quinazoline.

Avvertenze

Danger

Indicazioni di pericolo

H301 + H311 + H331,H373,H410

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

>446.0 °F

Punto d’infiammabilità (°C)

> 230 °C

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 4

1 of 4

2-Chloroaniline technical, ≥98.0% (GC)

Sigma-Aldrich

23310

2-Chloroaniline

2,5-Dibromoaniline 98%

Sigma-Aldrich

125881

2,5-Dibromoaniline

2-Chloroaniline for synthesis

Sigma-Aldrich

8.02611

2-Chloroaniline

3-(tert-Butyl)aniline AldrichCPR

Sigma-Aldrich

CDS013665

3-(tert-Butyl)aniline

Xiao-Feng Wu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(40), 12599-12602 (2012-09-05)
(C), its (O)K! An efficient palladium-catalyzed carbonylative synthesis of 2-alkylbenzoxazinones has been developed. By starting from 2-bromoanilines and acid anhydrides, the corresponding products were isolated in good yields.
Cobb JM, et al.
Tetrahedron Letters, 40(5), 1045-1048 (1999)
G O Rankin et al.
Journal of applied toxicology : JAT, 15(2), 139-146 (1995-03-01)
Haloanilines are commonly used as chemical intermediates in the manufacture of a wide range of products. The purpose of this study was to examine the in vivo nephrotoxic and hepatotoxic potentials of the 3-haloanilines. The in vitro effects of the
L A Khawli et al.
International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology, 19(3), 297-301 (1992-04-01)
Biotinyl-m-[125I]iodoanilide (BIA) was synthesized by coupling biotin to m-[125I]iodoaniline via a mixed anhydride reaction. m-[125I]Iodoaniline was produced from the tin precursor, which was prepared using a palladium catalyzed reaction of hexabutylditin with m-bromoaniline. The radioiodinated BIA derivative is characterized by
Ali Sarafraz Yazdi et al.
Journal of chromatography. A, 1082(2), 136-142 (2005-07-23)
A novel method for the extraction of aromatic amines present in water samples is produced here coupling two-step liquid-phase microextraction with high performance liquid chromatography by using a monolithic column. The hydrophobic porous polypropylene membranes were used as the interface

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.