259616
4-Chlorobenzhydrazide
98%
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| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 g | Check Cart for Availability | $33.80 |
About This Item
Linear Formula:
ClC6H4CONHNH2
CAS Number:
Molecular Weight:
170.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-632-0
Beilstein/REAXYS Number:
511154
MDL number:
Assay:
98%
Form:
solid
Quality Level
assay
98%
form
solid
mp
162-165 °C (lit.)
functional group
amine, chloro, hydrazine
SMILES string
NNC(=O)c1ccc(Cl)cc1
InChI
1S/C7H7ClN2O/c8-6-3-1-5(2-4-6)7(11)10-9/h1-4H,9H2,(H,10,11)
InChI key
PKBGHORNUFQAAW-UHFFFAOYSA-N
General description
Effect of acidic catalyst on the reaction of 4-chlorobenzhydrazide and β-naphthol in water has been investigated[1].
Application
4-Chlorobenzhydrazide has been used in preparation of:
- rod-shaped mesogenic hydrazide derivatives via Schotten-Baumann reaction with 4-n-alkoxybenzoyl chloride
- 4-methoxybenzaldehyde-4-chlorophenyl-1-carbonyl hydrazone
- 4-hydroxybenzaldehyde-4-chlorophenyl-1-carbonylhydrazone
- 2-nitrobenzaldehyde-4-chlorophenyl-1-carbonylhydrazone
- benzaldehyde-4-chlorophenyl-1-carbonylhydrazone
1 of 1
This Item | |||
|---|---|---|---|
| assay 98% | assay 98% | assay 98% | assay 98% |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| mp 162-165 °C (lit.) | mp 110-112 °C (lit.) | mp 149-150 °C (lit.) | mp 59-61 °C (lit.) |
| form solid | form powder | form powder | form crystals |
| functional group amine, hydrazine, chloro | functional group isothiocyanate, nitro | functional group carboxylic acid, chloro, ketone | functional group - |
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Jagvir Singh et al.
Bioinorganic chemistry and applications, 2012, 104549-104549 (2012-11-06)
N-substituted pyridine hydrazide (pyridine-2-carbonyl chloride and 4-chloro-benzoic acid hydrazide) undergoes hydrazide formation of the iminic carbon nitrogen double bond through its reaction with cobalt(II), nickel(II), and copper(II) metal salts in ethanol which are reported and characterized based on elemental analyses
Bent-shaped mesogenic oxadiazole and thiadiazole derivatives from rod-shaped mesogenic hydrazide containing polar chloro group.
Prajapati AK and Modi V.
Liq. Cryst., 37(4), 407-415 (2010)
Minoo Dabiri et al.
Bioorganic & medicinal chemistry letters, 18(1), 436-438 (2007-12-07)
Alkyl- or aryl-14H-dibenzo[a,j]xanthene derivatives are synthesized efficiently by the reaction of beta-naphthol and aliphatic and aromatic aldehydes in the presence of KAl(SO4)2 x 12 H2O (alum) under aqueous condition at 100 degrees C. Different types of aromatic and aliphatic aldehydes
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 259616-25G | 04061831838213 |
| 259616-5G | 04061826075371 |