25630
2-氯-6-硝基甲苯
purum, ≥99.0% (GC)
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关于此项目
线性分子式:
CH3C6H3(NO2)Cl
化学文摘社编号:
分子量:
171.58
EC Number:
201-475-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1239924
MDL number:
grade
purum
assay
≥99.0% (GC)
bp
238 °C (lit.)
mp
34-36 °C (lit.), 36-37 °C
solubility
methanol: soluble 1 g/10 mL, clear, colorless
SMILES string
Cc1c(Cl)cccc1[N+]([O-])=O
InChI
1S/C7H6ClNO2/c1-5-6(8)3-2-4-7(5)9(10)11/h2-4H,1H3
InChI key
XCSNRORTQRKCHB-UHFFFAOYSA-N
Application
2-Chloro-6-nitrotoluene has been used:
- as starting reagent in synthesis of 4-chloroindole-3-acetic acid and its esters
- in preparation of 2-chloro-6-aminobenzoic acid hydrochloride
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
257.0 °F
flash_point_c
125 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
A Synthesis of 2-Methoxy-8, 9-dichloroacridine Utilizing the Chapman Rearrangement.
Dauben WG and Hodgson RL.
Journal of the American Chemical Society, 72(8), 3479-3480 (1950)
M Katayama
Bioscience, biotechnology, and biochemistry, 64(4), 808-815 (2000-06-01)
4-Chloroindole-3-acetic acid (4-Cl-IAA) and its esters were synthesized from 2-chloro-6-nitrotoluene as the starting material. The biological activities of 4-CI-IAA and its esters were determined by four bioassays. Except for the tert-butyl ester, 4-Cl-IAA and its esters had stronger elongation activity
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