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259616

4-氯苯甲酰肼

Name: 4-氯苯甲酰肼
Brand: ALDRICH

98%

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关于此项目

线性分子式:

ClC₆H₄CONHNH₂

化学文摘社编号:

536-40-3

分子量:

170.60

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24855718

EC Number:

208-632-0

Beilstein/REAXYS Number:

511154

MDL number:

MFCD00007603

Assay:

98%

Form:

solid

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属性

Quality Level

100

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

说明

General description

Effect of acidic catalyst on the reaction of 4-chlorobenzhydrazide and β-naphthol in water has been investigated.

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

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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Synthesis, Spectroscopic Characterization, and In Vitro Antimicrobial Studies of Pyridine-2-Carboxylic Acid N'-(4-Chloro-Benzoyl)-Hydrazide and Its Co(II), Ni(II), and Cu(II) Complexes.

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

Eco-friendly and efficient one-pot synthesis of alkyl- or aryl-14H-dibenzo[a,j]xanthenes in water.

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

Synthesis of benzaldehyde substituted phenyl carbonyl hydrazones and their formylation using Vilsmeier-Haack reaction.

Rajput AP and Rajput AS.

International Journal of PharmTech Research, 1(4), 1605-1611 (2009)

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全球贸易项目编号

货号	GTIN
259616-25G	04061831838213
259616-5G	04061826075371