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Merck

137677

Sigma-Aldrich

2-溴苯甲酸

97%

别名:

邻溴苯甲酸

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About This Item

线性分子式:
BrC6H4CO2H
CAS号:
分子量:
201.02
Beilstein:
971266
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽壓力

>1 mmHg ( 20 °C)

化驗

97%

形狀

powder

mp

147-150 °C (lit.)

溶解度

95% ethanol: soluble 100 mg/mL, clear, colorless to yellow

SMILES 字串

OC(=O)c1ccccc1Br

InChI

1S/C7H5BrO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)

InChI 密鑰

XRXMNWGCKISMOH-UHFFFAOYSA-N

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一般說明

2-溴苯甲酸(2-BA)与氨基喹啉缩合,产生苯基喹啉胺。2-BA是合成各种氮杂环的常用结构单元

應用

2-溴苯甲酸被用于合成新型锌(II)-2-溴苯甲酸盐络合物。它被用作合成半不稳定的苯并咪唑基膦配体的起始试剂

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

>212.0 °F

閃點(°C)

> 100 °C

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Thermal decomposition and antimicrobial activity of zinc (II) 2-bromobenzoates with organic ligands.
Krajnikova A, et al.
Journal of Thermal Analysis and Calorimetry, 105(2), 451-460 (2011)
Free radical reactions for heterocycle synthesis. Part 6: 2-Bromobenzoic acids as building blocks in the construction of nitrogen heterocycles.
Zhang W and Pugh G.
Tetrahedron, 59(17), 3009-3018 (2003)
J B Bongui et al.
Chemical & pharmaceutical bulletin, 49(9), 1077-1080 (2001-09-18)
Condensation of either 2-bromobenzoic acid (4) or 2-chloro-3-nitrobenzoic acid (5) with suitable aminoquinolines 6-8 afforded phenylquinolylamines 9-13. Acid mediated cyclization gave the corresponding 12H-benzo[b][1,7]phenanthrolin-7-ones 14 and 15, and 12H-benzo[b][1,10]phenanthrolin-7-ones 16-18. Compounds 14, 16, and 17 were subsequently N-methylated to 6-demethoxyacronycine
Kin Ho Chung et al.
Chemical communications (Cambridge, England), 48(14), 1967-1969 (2012-01-12)
A new class of easily accessible hemilabile benzimidazolyl phosphine ligands has been developed. The ligand skeleton is prepared from commercially available and inexpensive o-phenylenediamine and 2-bromobenzoic acid. With catalyst loading down to 0.5 mol% palladium, excellent catalytic activity towards the
K H Engesser et al.
FEMS microbiology letters, 51(1), 143-147 (1989-07-15)
Pseudomonas putida strain CLB 250 (DSM 5232) utilized 2-bromo-, 2-chloro- and 2-fluorobenzoate as sole source of carbon and energy. Degradation is suggested to be initiated by a dioxygenase liberating halide in the first catabolic step. After decarboxylation and rearomatization catechol

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