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142158

1,3-二苯基脲

Name: 1,3-二苯基脲
Brand: ALDRICH

98%

别名:

N,N′-二苯脲, 碳酰苯胺

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关于此项目

线性分子式:

(C₆H₅NH)₂CO

化学文摘社编号:

102-07-8

分子量:

212.25

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24848383

EC Number:

203-003-7

Beilstein/REAXYS Number:

782650

MDL number:

MFCD00003017

Assay:

98%

Form:

powder

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属性

Quality Level

100

assay

98%

form

powder

bp

262 °C (lit.)

mp

239-241 °C (lit.)

solubility

pyridine: soluble 50 mg/mL, clear to very slightly hazy, colorless to faintly yellow

functional group

amine

SMILES string

O=C(Nc1ccccc1)Nc2ccccc2

InChI

1S/C13H12N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15,16)

InChI key

GWEHVDNNLFDJLR-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

说明

General description

1,3-二苯基脲是一种存在于水果和蔬菜中的细胞分裂素化合物。

Biochem/physiol Actions

1,3-二苯基脲由从内盖夫荒漠污染的短生沙漠河床分离的温和嗜盐菌海杆菌属代谢。

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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Metabolism of diphenylurea by a Marinobacter sp. isolated from a contaminated ephemeral stream bed in the Negev Desert.

Sebastian R Sørensen et al.

FEMS microbiology letters, 213(2), 199-204 (2002-08-09)

A moderate halophilic Marinobacter sp. (designated strain DPUZ) able to metabolize 1,3-diphenylurea (DPU) was isolated from a contaminated ephemeral desert stream bed near an industrial complex in the northern part of the Negev Desert (Israel). Metabolism of DPU was accompanied

Dispersive liquid-liquid microextraction for the determination of three cytokinin compounds in fruits and vegetables by liquid chromatography with time-of-flight mass spectrometry.

N Campillo et al.

Talanta, 116, 376-381 (2013-10-24)

The paper presents a novel approach for the determination of three cytokinin compounds, thidiazuron (TDZ), 1,3-diphenylurea (1,3-DPU) and forchlorfenuron (CPPU), in fruit and vegetables samples using liquid chromatography with electrospray ionization and time-of-flight mass spectrometry (LC-ESI-TOFMS). Analytes were extracted from

The structure-activity relationship of urea derivatives as anti-tuberculosis agents.

Joshua R Brown et al.

Bioorganic & medicinal chemistry, 19(18), 5585-5595 (2011-08-16)

The treatment of tuberculosis is becoming more difficult due to the ever increasing prevalence of drug resistance. Thus, it is imperative that novel anti-tuberculosis agents, with unique mechanisms of action, be discovered and developed. The direct anti-tubercular testing of a

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全球贸易项目编号

货号	GTIN
142158-25G	04061838734235
142158-100G	04061831828375