Detail of > 599-67-7
- CAS Number:
- 599-67-7
- Name:
1,1-Diphenylethanol
- Formula:
- C14H14O
- Molecular Structure:

- Synonyms:
- Benzhydrol,a-methyl- (6CI,7CI,8CI);1,1-Diphenyl-1-ethanol;Benzenemethanol, a-methyl-a-phenyl-;1-Hydroxy-1,1-diphenylethane;Diphenylmethylcarbinol;Methyldiphenylcarbinol;NSC 33;a-Methyl-a-phenylbenzenemethanol;a-Methylbenzhydrol;
- Molecular Weight:
- 198.2604
- EINECS:
- 209-970-1
- Density:
- 1.079 g/cm3
- Melting Point:
- 77-81 °C(lit.)
- Boiling Point:
- 328.2 ºC at 760 mmHg
- Flash Point:
- 141.4 ºC
- Appearance:
- white to off-white powder or needles
- Safety:
- 24/25Details
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Reference
- Structure of 1,1-diphenyl-1-ethanol
- Structure of 1,1-diphenyl-1-ethanol. Shnulin, A. N.; Sultanov, B. Yu.; Mamedov, Kh. S. (Azerb. Univ.In this article, certain chemicals are used. One of their cas registry numbers is 599-67-7 , Baku, USSR). Dokl. Akad. Nauk Az. SSR, 39(9), 48-9 (Russian) 1983. CODEN: DAZRA7. ISSN: 0002-3078. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) Section cross-reference(s): 75 X-ray diffraction indicated that Ph2CMeOH exists as H-bonded tetramers in the crystn. state, with 2 tetramers/unit cell. .
- Convenient synthesis of olefins from tertiary alcohols under mild basic condition
- Convenient synthesis of olefins from tertiary alcohols under mild basic condition. Li, Xin-Sheng; Ge, Jian-Feng; Hu, Xiao-Chun (Department of Chemistry and Biology, Zhejiang Normal University, Jinhua 321004, Peop. Rep. China). Youji Huaxue, 25(6), 727-729 (Chinese) 2005 Youji Huaxue Bianjibu. CODEN: YCHHDX. ISSN: 0253-2786. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) An efficient method has been achieved for the dehydration of tertiary alcs. using the combination of methanesulfonic anhydride and triethylamine as dehydration agent to obtain olefin in high yield.In this experiment, several chemicals are used like 599-67-7 The short reaction time, mild basic conditions and high yield make it a facile way for the synthesis of olefins from tertiary alcs. .
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