19486-60-3

• 

• Basic information

  1. Product Name: 2-Isopropyl-1,1'-biphenyl
  2. Synonyms: 2-(1-Methylethyl)-1,1'-biphenyl;2-Isopropyl-1,1'-biphenyl;2-Isopropylbiphenyl
  3. CAS NO:19486-60-3
  4. Molecular Formula: C₁₅H₁₆
  5. Molecular Weight: 196.2875
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 19486-60-3.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: 24.5°C
  2. Boiling Point: 269.77°C
  3. Flash Point: 140.2°C
  4. Appearance: /
  5. Density: 0.9811 (estimate)
  6. Refractive Index: 1.5761 (estimate)
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 2-Isopropyl-1,1'-biphenyl(CAS DataBase Reference)
  10. NIST Chemistry Reference: 2-Isopropyl-1,1'-biphenyl(19486-60-3)
  11. EPA Substance Registry System: 2-Isopropyl-1,1'-biphenyl(19486-60-3)

• 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: 19486-60-3(Hazardous Substances Data)

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

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19486-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19486-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,8 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19486-60:
(7*1)+(6*9)+(5*4)+(4*8)+(3*6)+(2*6)+(1*0)=143
143 % 10 = 3
So 19486-60-3 is a valid CAS Registry Number.

19486-60-3SDS

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	1-phenyl-2-propan-2-ylbenzene

1.2 Other means of identification

Product number	-
Other names	mono-isopropylbiphenyl

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:19486-60-3 SDS

19486-60-3Upstream product

• 98-82-8 Isopropylbenzene 
• 2396-01-2 phenyl radical 
• 17333-73-2 phenylium 
• 108-24-7 acetic anhydride 
• 643-28-7 2-isopropylaniline 
• 75-26-3 isopropyl bromide 
• 108-86-1 bromobenzene 
• 19099-54-8 2-isopropyliodobenzene 
• 92-52-4 biphenyl 
• 187737-37-7 propene 
• 66003-76-7 Diphenyliodonium triflate 

19486-60-3Downstream Products

• 50991-15-6 (+/-)-trans-2-Isopropyl-bicyclohexyl 
• 50991-15-6 (+/-)-cis-2-Isopropyl-bicyclohexyl 
• 7116-95-2 4-isopropylbiphenyl 

19486-60-3Relevant articles and documents

Palladium-catalyzed arylation of simple arenes with iodonium salts

Storr, Thomas E.,Greaney, Michael F.

supporting information, p. 1410 - 1413 (2013/05/09)

The development of an arylation protocol for simple arenes with diaryliodonium salts using the Herrmann-Beller palladacycle catalyst is reported. The reaction takes simple aromatic feedstocks and creates valuable biaryls for use in all sectors of the chem

Isopropylation of biphenyl over ZSM-12 zeolites

Chokkalingam, Anand,Kawagoe, Hiroaki,Watanabe, Seiji,Moriyama, Yasuhiro,Komura, Kenichi,Kubota, Yoshihiro,Kim, Jong-Ho,Seo, Gon,Vinu, Ajayan,Sugi, Yoshihiro

, p. 23 - 30 (2013/02/23)

ZSM-12 zeolites, ZSM-12L and ZSM-12S, with MTW topology were synthesized by using methyltriethylammonium bromide (MTEABr) and tetraethylammnoium bromide (TEABr) as structure directing agents (SDA), respectively, for the isopropylation of biphenyl (BP) usi

Synthesis of 4-alkyl-4-(4-methoxyphenyl)cyclohex-2-en-1-ones and 5-alkyl-5-phenyl-1,3-cyclohexadienes from bis(tricarbonylchromium)-coordinated biphenyls

Rieke, Reuben D.,Schulte, Louis D.,Dawson, Bryan T.,Yang, Sheng Sbeng

, p. 8388 - 8398 (2007/10/02)

(η6:η6-Biphenyl)[Cr(CO)3] 2 and (η6η64,4'-dimethoxybiphenyl) [Cr(CO)3]2 were chemically reduced with lithium anthracenide or lithium naphthalenide in THF to generate s

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