4-broMo-N1-Methylbenzene-1,2-diaMine
- Product Name
- 4-broMo-N1-Methylbenzene-1,2-diaMine
- CAS No.
- 69038-76-2
- Chemical Name
- 4-broMo-N1-Methylbenzene-1,2-diaMine
- Synonyms
- 5-bromo-2-(methylamino)aniline;4-broMo-N1-Methylbenzene-1,2-diaMine;4-Bromo-N1-methyl-1,2-benzenediamine;4-Bromo-1-N-methylbenzene-1,2-diamine;1,2-Benzenediamine, 4-bromo-N1-methyl-;tert-butyl 3-allyl-3-hydroxyazetidine-6-carboxylate
- CBNumber
- CB02715096
- Molecular Formula
- C7H9BrN2
- Formula Weight
- 201.06
- MOL File
- 69038-76-2.mol
4-broMo-N1-Methylbenzene-1,2-diaMine Property
- Boiling point:
- 298.2±30.0 °C(Predicted)
- Density
- 1.578±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C(protect from light)
- pka
- 5.48±0.11(Predicted)
- Appearance
- Light brown to brown Solid
- InChI
- InChI=1S/C7H9BrN2/c1-10-7-3-2-5(8)4-6(7)9/h2-4,10H,9H2,1H3
- InChIKey
- JGXCXQPNYWBAGW-UHFFFAOYSA-N
- SMILES
- C1(NC)=CC=C(Br)C=C1N
N-Bromosuccinimide Price
- Product number
- B613745
- Product name
- 4-Bromo-N1-methylbenzene-1,2-diamine
- Packaging
- 50mg
- Price
- $65
- Updated
- 2021/12/16
- Product number
- 150306
- Product name
- 4-Bromo-N1-methylbenzene-1,2-diamine
- Purity
- 95%
- Packaging
- 1g
- Price
- $196
- Updated
- 2021/12/16
- Product number
- 2680AJ
- Product name
- 4-Bromo-1-N-methylbenzene-1,2-diamine
- Packaging
- 10g
- Price
- $380
- Updated
- 2021/12/16
- Product number
- A135762
- Product name
- 4-Bromo-N1-methylbenzene-1,2-diamine
- Purity
- 97%
- Packaging
- 10g
- Price
- $390
- Updated
- 2021/12/16
- Product number
- 69038762
- Product name
- 4-Bromo-N1-methylbenzene-1,2-diamine
- Packaging
- 10g
- Price
- $395.2
- Updated
- 2021/12/16
4-broMo-N1-Methylbenzene-1,2-diaMine Chemical Properties,Usage,Production
Synthesis
53484-26-7
69038-76-2
General procedure for the synthesis of 4-bromo-N1-methylbenzene-1,2-diamine from 4-bromo-N-methyl-2-nitroaniline: to a solution of 4-bromo-N-methyl-2-nitroaniline (2.1 g, 9 mmol) in methanol (MeOH, 50 mL) was added iron powder (Fe, 2.5 g, 45 mmol) and ammonium chloride (NH4Cl, 4.8 g, 90 mmol). The reaction mixture was stirred at 80 °C for 4 hours. After completion of the reaction, the mixture was poured into water (H2O, 60 mL) and extracted with ethyl acetate (EA, 40 mL × 2). The organic layers were combined, dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to give 4-bromo-N1-methylbenzene-1,2-diamine (2.0 g, 99% yield) as a yellow solid.LC-MS m/z: 203.1 [M + H]+. Retention time (tR) = 1.64 min.
References
[1] Patent: WO2017/176960, 2017, A1. Location in patent: Paragraph 00743
[2] Patent: WO2012/119046, 2012, A2. Location in patent: Page/Page column 207
[3] Patent: WO2014/140075, 2014, A1. Location in patent: Page/Page column 231-232
[4] Patent: US6200976, 2001, B1
[5] Tetrahedron Letters, 2002, vol. 43, # 41, p. 7303 - 7306
4-broMo-N1-Methylbenzene-1,2-diaMine Preparation Products And Raw materials
Raw materials
Preparation Products
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