13703-52-1

• 

• Basic information

  1. Product Name: 2-Phenyl-1,4-cyclohexadiene
  2. Synonyms: 1,4-Cyclohexadienylbenzene;2-Phenyl-1,4-cyclohexadiene
  3. CAS NO:13703-52-1
  4. Molecular Formula: C₁₂H₁₂
  5. Molecular Weight: 156.2237
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 13703-52-1.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 237.4°Cat760mmHg
  3. Flash Point: 91.7°C
  4. Appearance: /
  5. Density: 1.006g/cm³
  6. Vapor Pressure: 0.0689mmHg at 25°C
  7. Refractive Index: 1.575
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2-Phenyl-1,4-cyclohexadiene(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2-Phenyl-1,4-cyclohexadiene(13703-52-1)
  12. EPA Substance Registry System: 2-Phenyl-1,4-cyclohexadiene(13703-52-1)

• 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: 13703-52-1(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• Benzene,1,4-cyclohexadien-1-yl-

  Cas No: 13703-52-1

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13703-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13703-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,0 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13703-52:
(7*1)+(6*3)+(5*7)+(4*0)+(3*3)+(2*5)+(1*2)=81
81 % 10 = 1
So 13703-52-1 is a valid CAS Registry Number.

InChI:InChI=1/C12H12/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1-5,7-8,10H,6,9H2

13703-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	cyclohexa-1,4-dien-1-ylbenzene

1.2 Other means of identification

Product number	-
Other names	1-Phenyl-cyclohexa-1,4-dien

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:13703-52-1 SDS

13703-52-1Upstream product

• 92-52-4 biphenyl 
• 54826-11-8 phenyltriene 
• 143-66-8 sodium tetraphenyl borate 
• 106-99-0 buta-1,3-diene 
• 536-74-3 phenylacetylene 
• 71-43-2 benzene 
• 15619-36-0 4-Chlor-1-phenyl-cyclohexen-1 
• 15619-39-3 O-(4-Phenyl-3-cyclohexenyl-⁽¹⁾)-S-methylxanthat 
• 2288-18-8 2-phenyl-1,3-butadiene 
• 41309-43-7 (2-bromovinyl)trimethylsilane 
• 152272-68-9 bis(9-borabicyclo{3.3.1}non-9-yl)acetylene 
• 401479-46-7 2-phenyl-2,3,6,7-tetrahydro-thiepine 1,1-dioxide 
• 80735-94-0 1-Phenyl-3-buten-1-ol 
• 654065-84-6 thioacetic acid S-(1-phenyl-but-3-enyl) ester 

13703-52-1Downstream Products

13703-52-1Relevant articles and documents

Catalysis by temporary covalent activation. A novel catalysis of unactivated Diels-Alder reactions

Singleton, Daniel A.,Leung, Shun-Wang,Martinez, Jose P.,Lee, Yu-Kai

, p. 3163 - 3166 (1997)

Diels-Alder reactions of cis-2-chlorovinyltributylstannane are greatly accelerated by the presence of catalytic amounts of haloboranes. Mechanistic studies support a mechanism for the catalysis involving an intermediate boron-aclivated dienophile. A simil

Synthesis of cyclic sulfones by ring-closing metathesis.

Yao, Qingwei

, p. 427 - 430 (2007/10/03)

A general and highly efficient synthesis of cyclic sulfones based on ring-closing metathesis has been developed. The synthetic utility of the resulting cyclic sulfones was demonstrated by their participation in stereoselective Diels-Alder reactions and transformation to cyclic dienes by the Ramberg-Baecklund reaction.

In situ formation of alkenyl- and alkynylboranes for Diels-Alder reactions by boron-silicon exchange with alkenyl- and alkynylsilanes

Singleton, Daniel A.,Leung, Shun-Wang

, p. 157 - 161 (2007/10/03)

A variety of alkenylsilanes underwent transmetallation with BBr3 to afford the corresponding alkenyldibromoboranes in solution. Similarly, the transmetallation of alkynylsilanes with BCl3 afforded alkynyldichloroboranes, A number of the alkenyl- and alkynylboranes are novel and useful Diels-Alder dienophiles. An ionic mechanism for the transmetallation is proposed.

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