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p,p'-bis(carbomethoxymethylamino)diphenylsulphone | 114710-04-2

分子结构分类

有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物

中文名称

——

中文别名

——

英文名称

p,p'-bis(carbomethoxymethylamino)diphenylsulphone

英文别名

p,p'-bis(carbmethoxymethylamino)diphenylsulphone；N,N'-(4,4'-sulfonyl-diphenyl)-bis-glycine dimethyl ester；N,N'-(4,4'-Sulfonyl-diphenyl)-bis-glycin-dimethylester；Bis-[4-(methoxycarbonylmethyl-amino)-phenyl]-sulfon；methyl 2-[4-[4-[(2-methoxy-2-oxoethyl)amino]phenyl]sulfonylanilino]acetate

p,p'-bis(carbomethoxymethylamino)diphenylsulphone化学式

CAS

114710-04-2

化学式

C₁₈H₂₀N₂O₆S

mdl

——

分子量

392.433

InChiKey

FDBOOPDCDLTFKW-UHFFFAOYSA-N

BEILSTEIN

——

EINECS

——

物化性质

熔点：

135 °C(Solvent: Dimethylformamide)
沸点：

573.6±45.0 °C(predicted)
密度：

1.354±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

辛醇/水分配系数(LogP)：

1.69
重原子数：

27.0
可旋转键数：

8.0
环数：

2.0
sp3杂化的碳原子比例：

0.22
拓扑面积：

110.8
氢给体数：

2.0
氢受体数：

8.0

上下游信息

上游原料

中文名称	英文名称	CAS号	化学式	分子量
氨苯砜	dapsone	80-08-0	C₁₂H₁₂N₂O₂S	248.305

下游产品

中文名称	英文名称	CAS号	化学式	分子量
——	2,2′-[sulfonylbis(1,4-phenyleneimino)]diaceticacid	7620-11-3	C₁₆H₁₆N₂O₆S	364.379
——	p,p'-Bis(hydrazinocarbonylmethylamino)diphenylsulphone	114710-05-3	C₁₆H₂₀N₆O₄S	392.439
——	p,p'-Bis(benzalhydrazinocarbonylmethylamino)diphenylsulphone	114710-06-4	C₃₀H₂₈N₆O₄S	568.656
——	[4-(4-{[(E)-3-Phenyl-prop-2-en-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [(E)-3-phenyl-prop-2-en-(Z)-ylidene]-hydrazide	114710-65-5	C₃₄H₃₂N₆O₄S	620.732
——	[4-(4-{[1-(4-Amino-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(4-amino-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-14-4	C₃₀H₃₀N₈O₄S	598.685
——	[4-(4-{[1-p-Tolyl-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-p-tolyl-meth-(Z)-ylidene]-hydrazide	114710-15-5	C₃₂H₃₂N₆O₄S	596.71
——	p,p'-bis(N-phenylureidocarbonylmethylamino)diphenylsulphone	116432-97-4	C₃₀H₂₈N₆O₆S	600.655
——	[4-(4-{[1-Pyridin-4-yl-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-pyridin-4-yl-meth-(Z)-ylidene]-hydrazide	114710-66-6	C₂₈H₂₆N₈O₄S	570.632
——	[4-(4-{[1-(4-Dimethylamino-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(4-dimethylamino-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-23-5	C₃₄H₃₈N₈O₄S	654.793
——	[4-(4-{[1-(3-Amino-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(3-amino-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-13-3	C₃₀H₃₀N₈O₄S	598.685
——	[4-(4-{[1-(4-Chloro-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(4-chloro-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-20-2	C₃₀H₂₆Cl₂N₆O₄S	637.546
——	p,p'-bis(N-phenylthioureidocarbonylmethylamino)diphenylsulphone	116433-23-9	C₃₀H₂₈N₆O₄S₃	632.788
——	[4-(4-{[1-(4-Hydroxy-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(4-hydroxy-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-08-6	C₃₀H₂₈N₆O₆S	600.655
——	N-[(4-methylphenyl)carbamoyl]-2-[4-[4-[[2-[(4-methylphenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-00-2	C₃₂H₃₂N₆O₆S	628.709
——	N-(benzylcarbamoyl)-2-[4-[4-[[2-(benzylcarbamoylamino)-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-15-9	C₃₂H₃₂N₆O₆S	628.709
——	N-[(4-hydroxyphenyl)carbamoyl]-2-[4-[4-[[2-[(4-hydroxyphenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-20-6	C₃₀H₂₈N₆O₈S	632.654
——	N-[(4-chlorophenyl)carbamoyl]-2-[4-[4-[[2-[(4-chlorophenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-09-1	C₃₀H₂₆Cl₂N₆O₆S	669.545
——	N-(benzylcarbamothioyl)-2-[4-[4-[[2-(benzylcarbamothioylamino)-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-40-0	C₃₂H₃₂N₆O₄S₃	660.842
——	N-[(4-methylphenyl)carbamothioyl]-2-[4-[4-[[2-[(4-methylphenyl)carbamothioylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-26-2	C₃₂H₃₂N₆O₄S₃	660.842
——	[4-(4-{[1-(4-Methoxy-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-16-6	C₃₂H₃₂N₆O₆S	628.709
——	4-[[2-[4-[4-[[2-oxo-2-[(4-sulfophenyl)carbamoylamino]ethyl]amino]phenyl]sulfonylanilino]acetyl]carbamoylamino]benzenesulfonic acid	116433-22-8	C₃₀H₂₈N₆O₁₂S₃	760.783
——	N-[(3-methylphenyl)carbamoyl]-2-[4-[4-[[2-[(3-methylphenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116432-99-6	C₃₂H₃₂N₆O₆S	628.709
——	[4-(4-{[1-(2-Chloro-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(2-chloro-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-19-9	C₃₀H₂₆Cl₂N₆O₄S	637.546
——	N-[(4-methoxyphenyl)carbamoyl]-2-[4-[4-[[2-[(4-methoxyphenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-03-5	C₃₂H₃₂N₆O₈S	660.707
——	N-[(4-hydroxyphenyl)carbamothioyl]-2-[4-[4-[[2-[(4-hydroxyphenyl)carbamothioylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-45-5	C₃₀H₂₈N₆O₆S₃	664.787
——	N-[(3-chlorophenyl)carbamoyl]-2-[4-[4-[[2-[(3-chlorophenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-08-0	C₃₀H₂₆Cl₂N₆O₆S	669.545
——	N-[(4-chlorophenyl)carbamothioyl]-2-[4-[4-[[2-[(4-chlorophenyl)carbamothioylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-35-3	C₃₀H₂₆Cl₂N₆O₄S₃	701.678
——	[4-(4-{[1-(2-Hydroxy-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(2-hydroxy-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-07-5	C₃₀H₂₈N₆O₆S	600.655
——	[4-(4-{[1-(4-Nitro-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(4-nitro-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-18-8	C₃₀H₂₆N₈O₈S	658.651
——	N-[(4-ethoxyphenyl)carbamoyl]-2-[4-[4-[[2-[(4-ethoxyphenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-18-2	C₃₄H₃₆N₆O₈S	688.761
——	4-[[2-[4-[4-[[2-oxo-2-[(4-sulfophenyl)carbamothioylamino]ethyl]amino]phenyl]sulfonylanilino]acetyl]carbamothioylamino]benzenesulfonic acid	116433-47-7	C₃₀H₂₈N₆O₁₀S₅	792.917
——	N-[(3-methylphenyl)carbamothioyl]-2-[4-[4-[[2-[(3-methylphenyl)carbamothioylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-25-1	C₃₂H₃₂N₆O₄S₃	660.842
——	N-[(4-methoxyphenyl)carbamothioyl]-2-[4-[4-[[2-[(4-methoxyphenyl)carbamothioylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-29-5	C₃₂H₃₂N₆O₆S₃	692.841
——	[4-(4-{[1-(2,4-Dichloro-phenyl)-meth-(Z)-ylidene-hydrazinocarbonylmethyl]-amino}-benzenesulfonyl)-phenylamino]-acetic acid [1-(2,4-dichloro-phenyl)-meth-(Z)-ylidene]-hydrazide	114710-21-3	C₃₀H₂₄Cl₄N₆O₄S	706.436
——	N-[(4-nitrophenyl)carbamoyl]-2-[4-[4-[[2-[(4-nitrophenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-12-6	C₃₀H₂₆N₈O₁₀S	690.65
——	N-[(3-chlorophenyl)carbamothioyl]-2-[4-[4-[[2-[(3-chlorophenyl)carbamothioylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-34-2	C₃₀H₂₆Cl₂N₆O₄S₃	701.678
——	N-(naphthalen-1-ylcarbamoyl)-2-[4-[4-[[2-(naphthalen-1-ylcarbamoylamino)-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-16-0	C₃₈H₃₂N₆O₆S	700.775
——	N-[(4-acetylphenyl)carbamoyl]-2-[4-[4-[[2-[(4-acetylphenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-14-8	C₃₄H₃₂N₆O₈S	684.729
——	N-[(2-bromophenyl)carbamoyl]-2-[4-[4-[[2-[(2-bromophenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-17-1	C₃₀H₂₆Br₂N₆O₆S	758.447
——	2,2'-((sulfonylbis(4,1-phenylene))bis(azanediyl))bis(N-(o-tolylcarbamoyl)acetamide)	116432-98-5	C₃₂H₃₂N₆O₆S	628.709
——	N-[(4-ethoxyphenyl)carbamothioyl]-2-[4-[4-[[2-[(4-ethoxyphenyl)carbamothioylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-43-3	C₃₄H₃₆N₆O₆S₃	720.894
——	4-[[2-[4-[4-[[2-[(4-carboxyphenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetyl]carbamoylamino]benzoic acid	116433-06-8	C₃₂H₂₈N₆O₁₀S	688.675
——	N-[(2-chlorophenyl)carbamoyl]-2-[4-[4-[[2-[(2-chlorophenyl)carbamoylamino]-2-oxoethyl]amino]phenyl]sulfonylanilino]acetamide	116433-07-9	C₃₀H₂₆Cl₂N₆O₆S	669.545

反应信息

作为反应物：

描述：

p,p'-bis(carbomethoxymethylamino)diphenylsulphone 在吡啶、一水合肼作用下，以 1,4-二氧六环、甲醇、乙醇为溶剂，反应 37.0h，生成

参考文献：

名称：

Shahsafi; Meshkatalsadat; Parekh, Journal of the Indian Chemical Society, 1988, vol. 65, # 1, p. 64 - 65

摘要：

DOI：
作为产物：

描述：

甲醇、 alkaline earth salt of/the/ methylsulfuric acid 在硫酸作用下，生成 p,p'-bis(carbomethoxymethylamino)diphenylsulphone

参考文献：

名称：

Sasosow; Iwanow, Zhurnal Obshchei Khimii, 1948, vol. 18, p. 227,229

摘要：

DOI：

点击查看最新优质反应信息

文献信息

Shahsafi, M. A.; Meshkatalsadat, M. H.; Parekh, Hansa, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1987, vol. 26, p. 803 - 807

作者：Shahsafi, M. A.、Meshkatalsadat, M. H.、Parekh, Hansa

DOI：——

日期：——
Meshkatalsadat, M. H.; Shahsafi, M. A.; Parekh, Hansa, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1988, vol. 27, # 1-12, p. 195 - 196

作者：Meshkatalsadat, M. H.、Shahsafi, M. A.、Parekh, Hansa

DOI：——

日期：——
Meshkatalsadat; Shahsafi; Parekh, Journal of the Indian Chemical Society, 1987, vol. 64, # 12, p. 768 - 770

作者：Meshkatalsadat、Shahsafi、Parekh

DOI：——

日期：——
MESHKATALSADAT, M. H.;SHAHSAFI, M. A.;PAREKH, HANSA, J. INST. CHEM., 61,(1989) N, C. 114-116

作者：MESHKATALSADAT, M. H.、SHAHSAFI, M. A.、PAREKH, HANSA

DOI：——

日期：——
MESHKATALSADAT, M. H.;SHAHSAFI, M. A.;PAREKH, HANSA, J. INDIAN CHEM. SOC., 64,(1987) N 12, 768-770

作者：MESHKATALSADAT, M. H.、SHAHSAFI, M. A.、PAREKH, HANSA

DOI：——

日期：——