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532878

Sigma-Aldrich

4-溴-3-甲基苯甲酸甲酯

95%

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About This Item

线性分子式:
BrC6H3(CH3)CO2CH3
CAS号:
148547-19-7
分子量:
229.07
MDL號碼:
MFCD00673014
分類程式碼代碼:
12352100
PubChem物質ID:
24877922
NACRES:
NA.22

品質等級

100

化驗

95%

mp

38-44 °C (lit.)

官能基

bromo
ester

SMILES 字串

COC(=O)c1ccc(Br)c(C)c1

InChI

1S/C9H9BrO2/c1-6-5-7(9(11)12-2)3-4-8(6)10/h3-5H,1-2H3

InChI 密鑰

GTZTYNPAPQKIIR-UHFFFAOYSA-N

相关类别

一般說明

Methyl 4-bromo-3-methylbenzoate, an aromatic ester, undergoes Suzuki coupling with 2-chloroboronic acid to afford the corresponding biaryl.

應用

Methyl 4-bromo-3-methylbenzoate may be used in the preparation of:
  • 4-bromo-3-vinylbenzoic acid
  • 4-bromo-3-(methylphenyl)methanol
  • methyl (E)-4-bromo-3-[(phenylmethoxyimino)methyl]benzoate

It may be used as a starting material in the total synthesis of (-)-martinellic acid.

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number
MKCK9179
MKCH0717
MKCC8513
MKBZ5902V
MKBR5897V

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Sigma-Aldrich

276855

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The asymmetric total synthesis of martinellic acid, the first pyrrolo[3,2-c]quinoline alkaloid found in nature, is described. Three key steps in our synthesis of (-)-martinellic acid are the Bu(3)SnH-promoted radical addition-cyclization-elimination (RACE) reaction of an oxime ether with an alpha,beta-unsaturated ester
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