主要文件

查看所有文档

B9602

二苯甲酮腙

Name: 二苯甲酮腙
Brand: ALDRICH

96%

别名:

二苯基重氮甲烷前体

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:

(C₆H₅)₂C=NNH₂

化学文摘社编号:

5350-57-2

分子量:

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

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

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

说明

pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

294.8 °F

flash_point_c

146 °C

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

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

查看所有相关文献

全球贸易项目编号

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