C23802
4-Chlorobenzamide
98%
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About This Item
Linear Formula:
ClC6H4CONH2
CAS Number:
Molecular Weight:
155.58
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
solid
mp
172-176 °C (lit.)
SMILES string
NC(=O)c1ccc(Cl)cc1
InChI
1S/C7H6ClNO/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H2,9,10)
InChI key
BLNVISNJTIRAHF-UHFFFAOYSA-N
Related Categories
1 of 4
This Item | 308560 | 499234 | 128740 |
|---|---|---|---|
| assay 97% | assay 98% | assay 98% | assay 97% |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| solubility acetic acid: soluble 50 mg/mL, clear, colorless to faintly yellow | solubility - | solubility - | solubility - |
| form solid | form powder | form - | form - |
| mp 183-186 °C (lit.) | mp 257-261 °C (lit.) | mp 30-34 °C (lit.) | mp 157-159 °C (lit.) |
| functional group chloro | functional group chloro | functional group ketone | functional group - |
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Influence of chlorine-substitution in pyrimidine ring on proton donor ability in H-bond and parameters of amino group of 2-amino pyrimidine.
Borisenko VE, et al.
Vibrational Spectroscopy, 37(1), 97-109 (2005)
T Jayavarthanan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 97, 811-824 (2012-08-21)
The solid phase FTIR and FT-Raman spectra of 2-amino-4-chloro-6-methylpyrimidine (2A4Cl6MP) have been recorded in the regions 400-4000 and 50-4,000 cm(-1), respectively. The spectra have been interpreted interms of fundamentals modes, combination and overtone bands. The structure of the molecule has
J A Hutter et al.
Biochemistry, 26(7), 1969-1973 (1987-04-07)
Thiaminase I from Bacillus thiaminolyticus strain Matsukawa et Misawa is completely and irreversibly inhibited by treatment with 4-amino-6-chloro-2-methylpyrimidine. Inhibition is a time-dependent first-order process, exhibiting a half-time of 4 h at an inhibitor concentration of 5 mM. A specific active-site-directed
Effects of nitrification inhibitors on denitrification of nitrate in soil.
Bremner JM andYeomans JC.
Biology and Fertility of Soils, 2(4), 173-179 (1986)
Christer B Aakeröy et al.
Pharmaceutics, 3(3), 601-614 (2011-01-01)
In the pharmaceutical industry, co-crystals are becoming increasingly valuable as crystalline solids that can offer altered/improved physical properties of an active pharmaceutical ingredient (API) without changing its chemical identity or biological activity. In order to identify new solid forms of
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