10442-33-8

• 

• Basic information

  1. Product Name: 3,4-diphenylhexane-3,4-diol
  2. Synonyms:
  3. CAS NO:10442-33-8
  4. Molecular Formula: C₁₈H₂₂O₂
  5. Molecular Weight: 270.3661
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 10442-33-8.mol
  9. Article Data: 10

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 418.6°C at 760 mmHg
  3. Flash Point: 192.4°C
  4. Appearance: N/A
  5. Density: 1.1g/cm³
  6. Vapor Pressure: 9.37E-08mmHg at 25°C
  7. Refractive Index: 1.573
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 3,4-diphenylhexane-3,4-diol(CAS DataBase Reference)
  11. NIST Chemistry Reference: 3,4-diphenylhexane-3,4-diol(10442-33-8)
  12. EPA Substance Registry System: 3,4-diphenylhexane-3,4-diol(10442-33-8)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 10442-33-8(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• 3,4-diphenylhexane-3,4-diol

  Cas No: 10442-33-8

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

• Dayang Chem (Hangzhou) Co.,Ltd.
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• 3,4-diphenylhexane-3,4-diol

  Cas No: 10442-33-8

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• Hangzhou J&H Chemical Co., Ltd.
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• 10442-33-8

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• Henan Tianfu Chemical Co., Ltd.
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• 3,4-diphenylhexane-3,4-diol cas 10442-33-8

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• Hangzhou Fandachem Co.,Ltd
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• 3,4-diphenylhexane-3,4-diol

  Cas No: 10442-33-8

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• Shanghai united Scientific Co.,Ltd.
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10442-33-8 Usage

General Description

3,4-diphenylhexane-3,4-diol is a chemical compound with the molecular formula C18H22O2. It is a diol, which means it contains two hydroxyl (-OH) functional groups. 3,4-diphenylhexane-3,4-diol is a colorless, odorless, and viscous liquid. It is often used as a reagent in organic synthesis and can also serve as an intermediate in the production of other chemicals. In addition, 3,4-diphenylhexane-3,4-diol has potential applications in the production of polymers and as a building block for the synthesis of various organic compounds. Its versatile properties make it a valuable compound in the field of organic chemistry and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 10442-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10442-33:
(7*1)+(6*0)+(5*4)+(4*4)+(3*2)+(2*3)+(1*3)=58
58 % 10 = 8
So 10442-33-8 is a valid CAS Registry Number.

10442-33-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	3,4-diphenylhexane-3,4-diol

1.2 Other means of identification

Product number	-
Other names	3,4-diphenyl-hexane-3,4-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10442-33-8 SDS

10442-33-8Upstream product

• 64-17-5 ethanol 
• 93-55-0 1-phenyl-propan-1-one 
• 60-29-7 diethyl ether 
• 54589-41-2 (4-(benzyloxy)phenyl)(phenyl)methanone 
• 98-85-1 1-Phenylethanol 
• 1636-34-6 2,3-diphenyl-2,3-butanediol 
• 98-86-2 acetophenone 
• 93-54-9 1-Phenyl-1-propanol 

10442-33-8Downstream Products

• 93-55-0 1-phenyl-propan-1-one 
• 24815-65-4 (E,E)-3,4-diphenyl-2,4-hexadiene 

10442-33-8Relevant articles and documents

Quenching of Triplet Ketones by Alcohol OH Bonds

Wagner, Peter J.,Puchalski, Allen E.

, p. 7138 - 7140 (1980)

-

-

Masuura,Kitaura

, p. 2483 (1968)

-

-

Stocker,Jenevein

, p. 2145 (1968)

-

The first oxidative addition of a hypervalent compound to metallic lanthanoid: Synthesis, characterization, and reaction of samarium(ii) bis(trifluoromethanesulfonate) derived from metallic samarium and 1, 5-dithioniabicyclo[3.3.0]octane bis(trifluorometh

Mashima, Kazushi,Oshiki, Toshiyuki,Tani, Kazuhide

, p. 7114 - 7116 (1998)

-

Enantioselective cathodic reduction of some prochiral ketones in the presence of (1R,2S)-(-)-N,N-dimethylephedrinium tetrafluoroborate at a mercury pool cathode

Yadav, Ashok K.,Singh, Arpita

, p. 587 - 588 (2007/10/03)

The enantioselective cathodic reduction of some prochiral ketones viz. acetophenone (I), propiophenone (II), butyrophenone (III), valerophenone (IV), isobutyrophenone (V), and pivalophenone (VI) has been accomplished at a mercury pool cathode in N,N-dimethylformamide (DMF)-water (90:10) using tetrabutylammonium fluoroborate (TBA·BF4) as a supporting electrolyte in the presence of (1R,2S)-(-)-N,N-dimethylephedrinium tetrafluoroborate (DET). Cyclic voltammetric investigations have been carried out and a probable mechanism of the process has been presented.

Preparation of Samarium(II) Triflate and It Mediated Grignard-type Reaction. In Situ Formation and Reaction of New Organosamarium Reagents

Fukuzawa, Shin-ichi,Tsuchimoto, Teruhisa,Kanai, Takeshi

, p. 1981 - 1984 (2007/10/02)

Samarium(II) triflate was readily prepared by reaction of samarium(III) triflate with sec-butyllithium at room temperature in THF.Its reducing ability was examined by pinacol coupling of carbonyl compounds.Sm(OTf)2 mediated Grignard-type reaction in THF-HMPA effectively; alkylation and allylation of ketones or aldehydes by simple alkyl, allyl, and benzyl halides proceeded via organosamarium intermediates.

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