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o-isobutyltoluene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 36301-29-8 Structure
  • Basic information

    1. Product Name: o-isobutyltoluene
    2. Synonyms: o-isobutyltoluene;2-Isobutyltoluene
    3. CAS NO:36301-29-8
    4. Molecular Formula: C11H16
    5. Molecular Weight: 148.24474
    6. EINECS: 252-957-0
    7. Product Categories: N/A
    8. Mol File: 36301-29-8.mol
  • Chemical Properties

    1. Melting Point: -73.3°C
    2. Boiling Point: 196°C
    3. Flash Point: 68.6°C
    4. Appearance: /
    5. Density: 0.8610
    6. Vapor Pressure: 0.572mmHg at 25°C
    7. Refractive Index: 1.4912
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: o-isobutyltoluene(CAS DataBase Reference)
    11. NIST Chemistry Reference: o-isobutyltoluene(36301-29-8)
    12. EPA Substance Registry System: o-isobutyltoluene(36301-29-8)
  • 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: 36301-29-8(Hazardous Substances Data)

36301-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36301-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,0 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36301-29:
(7*3)+(6*6)+(5*3)+(4*0)+(3*1)+(2*2)+(1*9)=88
88 % 10 = 8
So 36301-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16/c1-9(2)8-11-7-5-4-6-10(11)3/h4-7,9H,8H2,1-3H3

36301-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-isobutyl-2-methyl-benzene

1.2 Other means of identification

Product number -
Other names Benzene, 1-methyl-2-(2-methylpropyl)-

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:36301-29-8 SDS

36301-29-8Downstream Products

36301-29-8Relevant articles and documents

Catalytic Intermolecular C(sp3)-H Amination: Selective Functionalization of Tertiary C-H Bonds vs Activated Benzylic C-H Bonds

Brunard, Erwan,Boquet, Vincent,Van Elslande, Elsa,Saget, Tanguy,Dauban, Philippe

, p. 6407 - 6412 (2021/05/29)

A catalytic intermolecular amination of nonactivated tertiary C(sp3)-H bonds (BDE of 96 kcal·mol-1) is reported for substrates displaying an activated benzylic site (BDE of 85 kcal·mol-1). The tertiary C(sp3)-H bond is selectively functionalized to afford α,α,α-Trisubstituted amides in high yields. This unusual site-selectivity results from the synergistic combination of Rh2(S-Tfpttl)4, a rhodium(II) complex with a well-defined catalytic pocket, with tert-butylphenol sulfamate (TBPhsNH2), which leads to a discriminating rhodium-bound nitrene species under mild oxidative conditions. This catalytic system is very robust, and the reaction was performed on a 50 mmol scale with only 0.01 mol % of catalyst. The TBPhs group can be removed under mild conditions to afford the corresponding NH-free amines.

An N-heterocyclic carbene-based nickel catalyst for the Kumada–Tamao–Corriu coupling of aryl bromides and tertiary alkyl Grignard reagents

Ando, Shin,Mawatari, Mai,Matsunaga, Hirofumi,Ishizuka, Tadao

supporting information, p. 3287 - 3290 (2016/07/11)

In this study, nickel-catalyzed coupling reactions between arylhalides and tert-alkyl Grignard reagents were developed. Our original bicyclic NHC ligands reduced the formation of isomerized products, and we found that NMP as a co-solvent suppressed the reduction process. Under the optimal conditions we developed, the catalyst loading was lowered to 0.5?mol?%, and catalyst loading using ortho-substituted aryl bromides was also applicable at the level of 2.0?mol?%.

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