1657-60-9 (Benzenemethanol, 伪-(1,1-dimethylethyl)-伪-phenyl-,tert-Butyldiphenylmethanol)

CAS号:
1657-60-9
中文名称:
Benzenemethanol, 伪-(1,1-dimethylethyl)-伪-phenyl-
英文名称:
tert-Butyldiphenylmethanol
分子式:
C17H20O
分子量:
240.340105056763

Benzenemethanol, 伪-(1,1-dimethylethyl)-伪-phenyl-(1657-60-9)名称与标识符

名称

中文别名:
Benzenemethanol, 伪-(1,1-dimethylethyl)-伪-phenyl-;
英文别名:
2,2-dimethyl-1,1-diphenylpropan-1-ol;A-TERT-BUTYLBENZHYDROL;TERT-BUTYLDIPHENYLMETHANOL;1-Hydroxy-2.2-dimethyl-1.1-diphenyl-propan;2,2-Dimethyl-1,1-diphenyl-1-propanol;2,2-dimethyl-1,1-diphenyl-propan-1-ol;t-Butyldiphenylmethanol;tert.-Butyl-diphenyl-carbinol;Tert-ButyldiPhenyl-Methanol;TIMTEC-BB SBB008327;ALPHA-TERT-BUTYLBENZHYDROL;2,2-dimethyl-1,1-di(phenyl)propan-1-ol;Benzenemethanol, ;A-(1,1-dimethylethyl)-;A-phenyl-;1,1-Diphenyl-2,2-dimethyl-1-propanol;2,2-Dimethyl-1,1-diphenyl-1-propanol #;FT-0622500;AKOS015837801;SCHEMBL15275691;DTXSID60168014;YOVSPPKJDDWJML-UHFFFAOYSA-N;1657-60-9;MFCD00043743;

标识符

MDL:
MFCD00043743
InChIKey:
YOVSPPKJDDWJML-UHFFFAOYSA-N
Inchi:
1S/C17H20O/c1-16(2,3)17(18,14-10-6-4-7-11-14)15-12-8-5-9-13-15/h4-13,18H,1-3H3
SMILES:
OC(C1C=CC=CC=1)(C1C=CC=CC=1)C(C)(C)C

Benzenemethanol, 伪-(1,1-dimethylethyl)-伪-phenyl-(1657-60-9)物化性质

实验特性

  • LogP : 3.96860
  • PSA : 20.23000

计算特性

  • 精确分子量 : 240.15100
  • 氢键供体数量 : 1
  • 氢键受体数量 : 1
  • 可旋转化学键数量 : 3
  • 同位素质量 : 240.151415257g/mol
  • 重原子数量 : 18
  • 复杂度 : 233
  • 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) : 4.3
  • 拓扑分子极性表面积 : 20.2

Benzenemethanol, 伪-(1,1-dimethylethyl)-伪-phenyl-(1657-60-9)海关数据

海关编码:
2906299090
海关数据:

中国海关编码:

2906299090

概述:

2906299090 其他芳香醇. 增值税率:17.0% 退税率:9.0% 监管条件:无 最惠国关税:5.5% 普通关税:30.0%

申报要素:

品名, 成分含量, 用途

Summary:

2906299090 other aromatic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Benzenemethanol, 伪-(1,1-dimethylethyl)-伪-phenyl-(1657-60-9)相关文献

  • 1. Reactions of 2,2-dimethyl-1,1-diphenylpropan-1-ol with acidic reagents: a reinvestigation of the dehydration products and isolation of a sulphonation product
    Heather Scott,Roy Shilton J. Chem. Soc. Perkin Trans. 1 1977 247
  • 2. 529. Insecticidal activity and chemical constitution. Part III. A° new synthetic route to methyl analogues of DDT
    E. John Skerrett,D. Woodcock J. Chem. Soc. 1952 2804
  • 3. Reactions of lead tetra-acetate. Part XIII. Homolytic and heterolytic mechanisms in the oxidation of alcohols
    R. O. C. Norman,R. A. Watson J. Chem. Soc. B 1968 692
  • 4. Azo anions in synthesis: α-amino carbanion equivalents from t-butyldiphenyl-methylhydrazones
    Jack E. Baldwin,Robert M. Adlington,Ian M. Newington J. Chem. Soc. Chem. Commun. 1986 176