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B9602

Benzophenone hydrazone

Name: Benzophenone hydrazone
Brand: ALDRICH

96%

Synonym(s):

Diphenyldiazomethane precursor

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About This Item

Linear Formula:

(C₆H₅)₂C=NNH₂

CAS Number:

5350-57-2

Molecular Weight:

196.25

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24892146

EC Number:

226-321-8

Beilstein/REAXYS Number:

1910177

MDL number:

MFCD00007624

Assay:

96%

Form:

crystals

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Properties

Quality Level

100

assay

96%

form

crystals

bp

225-230 °C/55 mmHg (lit.)

mp

95-98 °C (lit.)

storage temp.

2-8°C

SMILES string

N\N=C(/c1ccccc1)c2ccccc2

InChI

1S/C13H12N2/c14-15-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,14H2

InChI key

QYCSNMDOZNUZIT-UHFFFAOYSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

294.8 °F

flash_point_c

146 °C

ppe

Eyeshields, Gloves, type N95 (US)

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Synthesis and urease inhibitory potential of benzophenone sulfonamide hybrid in vitro and in silico.

Arshia et al.

Bioorganic & medicinal chemistry, 27(6), 1009-1022 (2019-02-11)

This study deals with the synthesis of benzophenone sulfonamides hybrids (1-31) and screening against urease enzyme in vitro. Studies showed that several synthetic compounds were found to have good urease enzyme inhibitory activity. Compounds 1 (N'-((4'-hydroxyphenyl)(phenyl)methylene)-4''-nitrobenzenesulfonohydrazide), 2 (N'-((4'-hydroxyphenyl)(phenyl)methylene)-3''-nitrobenzenesulfonohydrazide), 3 (N'-((4'-hydroxyphenyl)(phenyl)methylene)-4''-methoxybenzenesulfonohydrazide)

Paired Utility of Aza-Amino Acyl Proline and Indolizidinone Amino Acid Residues for Peptide Mimicry: Conception of Prostaglandin F2α Receptor Allosteric Modulators That Delay Preterm Birth.

Fatemeh M Mir et al.

Journal of medicinal chemistry, 62(9), 4500-4525 (2019-04-02)

Peptide mimicry employing a combination of aza-amino acyl proline and indolizidinone residues has been used to develop allosteric modulators of the prostaglandin F2α receptor. The systematic study of the N-terminal phenylacetyl moiety and the conformation and side chain functions of

Influences of Histidine-1 and Azaphenylalanine-4 on the Affinity, Anti-inflammatory, and Antiangiogenic Activities of Azapeptide Cluster of Differentiation 36 Receptor Modulators.

Kelvine Chignen Possi et al.

Journal of medicinal chemistry, 60(22), 9263-9274 (2017-10-14)

Azapeptide analogues of growth hormone releasing peptide-6 (GHRP-6) exhibit promising affinity, selectivity, and modulator activity on the cluster of differentiation 36 receptor (CD36). For example, [A

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Global Trade Item Number

SKU	GTIN
B9602-100G	04061838352811
B9602-500G	04061832107684