24067-35-4 (N-(2-氯苯基)胍,N-(2-CHLORO-PHENYL)-GUANIDINE)

CAS号:
24067-35-4
中文名称:
N-(2-氯苯基)胍
英文名称:
N-(2-CHLORO-PHENYL)-GUANIDINE
分子式:
C7H8ClN3
分子量:
169.611519813538

N-(2-氯苯基)胍(24067-35-4)名称与标识符

名称

中文别名:
2'-氯苯基胍;N-(2-氯苯基)胍;
英文别名:
N-(2-CHLORO-PHENYL)-GUANIDINE;2-(2-chlorophenyl)guanidine;N-(2-Chlorophenyl)guanidine;N-(2-chlorophenyl)-guanidine;N-(2-Chlorphenyl)guanidin;o-chlorophenylguanidine;o-Chlorphenyl-guanidin;CS-0450250;HKPHVFFQXHMOHX-UHFFFAOYSA-N;1N-amino(immino)methyl-2-chloroaniline;J-015339;1-(2-chlorophenyl)guanidine;DTXSID80482582;PD129932;J-522897;BDBM50053633;SCHEMBL1187007;CHEMBL41853;SB36019;AKOS011667952;24067-35-4;

标识符

MDL:
MFCD04114640
InChIKey:
HKPHVFFQXHMOHX-UHFFFAOYSA-N
Inchi:
1S/C7H8ClN3/c8-5-3-1-2-4-6(5)11-7(9)10/h1-4H,(H4,9,10,11)
SMILES:
ClC1C=CC=CC=1/N=C(\N)/N

N-(2-氯苯基)胍(24067-35-4)物化性质

实验特性

  • LogP : 2.51840
  • PSA : 61.90000

计算特性

  • 精确分子量 : 169.04100
  • 氢键供体数量 : 3
  • 氢键受体数量 : 3
  • 可旋转化学键数量 : 2
  • 同位素质量 : 169.0406750g/mol
  • 重原子数量 : 11
  • 复杂度 : 154
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 1
  • 拓扑分子极性表面积 : 64.4Ų

N-(2-氯苯基)胍(24067-35-4)海关数据

海关编码:
2925290090
海关数据:

中国海关编码:

2925290090

概述:

2925290090 其他亚胺及其衍生物,以及它们的盐。监管条件:无。增值税率:17.0%。退税率:9.0%。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

Summary:

2925290090 other imines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

N-(2-氯苯基)胍(24067-35-4)推荐厂家 更多厂家(5)

公司名称手机号/电话联系人QQ微信询单
金锦乐(湖南)化学有限公司 金锦乐 1226360695
询单
上海甄准生物科技有限公司 15102117276
021-68920155
姜经理15102117276 3001090745
询单
上海瀚思化工有限公司 18939883912
021-34536277
顾经理 3003949364
询单
江苏倍达医药科技有限公司 18994340901
0512-63009836
贺慧 540534176 询单

N-(2-氯苯基)胍(24067-35-4)相关文献

  • 1. 540. Synthetic antimalarials. Part XLV. Reactions between monosubstituted cyanoguanidines and grignard reagents leading to N-p-chlorophenylguanylamidines
    Stanley Birtwell J. Chem. Soc. 1949 2561
  • 2. 540. Synthetic antimalarials. Part XLV. Reactions between monosubstituted cyanoguanidines and grignard reagents leading to N-p-chlorophenylguanylamidines
    Stanley Birtwell J. Chem. Soc. 1949 2561
  • 3. 540. Synthetic antimalarials. Part XLV. Reactions between monosubstituted cyanoguanidines and grignard reagents leading to N-p-chlorophenylguanylamidines
    Stanley Birtwell J. Chem. Soc. 1949 2561
  • 4. 121. Synthetic antimalarials. Part XXV. Some 4-arylguanidino-2- and -6-dialkylaminoalkylaminopyrimidines
    A. F. Crowther,F. H. S. Curd,F. L. Rose J. Chem. Soc. 1948 586
  • 5. 539. Synthetic antimalarials. Part XLIV. The preparation of diguanides by the reaction of substituted amino-(including guanidino-)magnesium halides with the 〉N·CN group
    S. Birtwell,F. H. S. Curd,F. L. Rose J. Chem. Soc. 1949 2556
  • 6. 539. Synthetic antimalarials. Part XLIV. The preparation of diguanides by the reaction of substituted amino-(including guanidino-)magnesium halides with the 〉N·CN group
    S. Birtwell,F. H. S. Curd,F. L. Rose J. Chem. Soc. 1949 2556
  • 7. A captured room temperature stable Wheland intermediate as a key structure for the orthogonal decoration of 4-amino-pyrido[2,3-d]pyrimidin-7(8H)-ones
    I?aki Galve,Raül Ondo?o,Claudi de Rocafiguera,Raimon Puig de la Bellacasa,Xavier Batllori,Cristina Puigjaner,Mercè Font-Bardia,Oriol Vallcorba,Jordi Teixidó,José I. Borrell Org. Biomol. Chem. 2020 18 9810
  • 8. 231. Attempts to prepare a possible metabolite of “Paludrine”(proguanil) and related 1 : 3 : 5-triazines
    Stanley Birtwell J. Chem. Soc. 1952 1279
  • 9. 53. Synthetic antimalarials. Part XXXIV. Physicochemical studies on the diguanides
    J. C. Gage J. Chem. Soc. 1949 221
  • 10. 611. Arylamides of halogenated methane- and ethane-sulphonic acids
    W. V. Farrar J. Chem. Soc. 1960 3058