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3’,4-二氨基苯酰替苯胺

更新时间:2025-09-15 18:19:52

3’,4-二氨基苯酰替苯胺结构式
3’,4-二氨基苯酰替苯胺结构式
品牌特惠专场
常用名 3’,4-二氨基苯酰替苯胺 英文名 Benzamide,4-amino-N-(3-aminophenyl)
CAS号 2657-85-4 分子量 227.26200
密度 1.314g/cm3 沸点 383.7ºC at 760mmHg
分子式 C13H13N3O 熔点 N/A
MSDS N/A 闪点 N/A

 3’,4-二氨基苯酰替苯胺名称

中文名 3’,4-二氨基苯酰替苯胺
英文名 4-Amino-N-(3-aminophenyl)benzamide
中文别名 3`,4-二氨基苯酰替苯胺 | 4-氨基-N-(3-氨基苯基)-苯甲酰胺
英文别名 更多

 3’,4-二氨基苯酰替苯胺物理化学性质

密度 1.314g/cm3
沸点 383.7ºC at 760mmHg
分子式 C13H13N3O
分子量 227.26200
精确质量 227.10600
PSA 81.14000
LogP 3.33870
InChIKey HWKHQQCBFMYAJZ-UHFFFAOYSA-N
SMILES Nc1ccc(C(=O)Nc2cccc(N)c2)cc1
蒸汽压 4.31E-06mmHg at 25°C
折射率 1.734

 3’,4-二氨基苯酰替苯胺安全信息

海关编码 2924299090

 3’,4-二氨基苯酰替苯胺合成线路

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3’,4-二氨基苯酰替苯胺结构式

3’,4-二氨基苯酰替苯胺

2657-85-4

文献:Ges. f. chem. Ind. Basel Patent: DE221433 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 10, p. 912

~%

3’,4-二氨基苯酰替苯胺结构式

3’,4-二氨基苯酰替苯胺

2657-85-4

文献:Ges. f. chem. Ind. Basel Patent: DE221433 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 10, p. 912

~%

3’,4-二氨基苯酰替苯胺结构式

3’,4-二氨基苯酰替苯胺

2657-85-4

文献:Ges. f. chem. Ind. Basel Patent: DE221433 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 10, p. 912

 3’,4-二氨基苯酰替苯胺上下游产品

3’,4-二氨基苯酰替苯胺上游产品  3

3’,4-二氨基苯酰替苯胺下游产品  0

 3’,4-二氨基苯酰替苯胺海关

海关编码 2924299090
中文概述 2924299090. 其他环酰胺(包括环氨基甲酸酯)(包括其衍生物以及他们的盐). 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%
申报要素 品名, 成分含量, 用途, 包装
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 3’,4-二氨基苯酰替苯胺靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
实验名称:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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 3’,4-二氨基苯酰替苯胺英文别名

Benzanilide,4-diamino
3,4'-Diaminobenzanilid
3',4-Diaminobenzanilide
4,3'-diaminobenzanilide
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