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Benzene, 2-methoxy-4-methyl-1-(1-methylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 39701-08-1 Structure
  • Basic information

    1. Product Name: Benzene, 2-methoxy-4-methyl-1-(1-methylethenyl)-
    2. Synonyms: 2-(2-Methoxy-4-methylphenyl)prop-1-ene;2-(2-methoxy-4-methylphenyl)propene;Benzene,2-methoxy-4-methyl-1-(1-methylethenyl);Methyl-(3-methyl-6-isopropenyl-phenyl)-aether;2-isopropenyl-5-methyl-anisole;3-Methoxy-1-methyl-4-isopropenyl-benzol;2-Isopropenyl-5-methyl-anisol;1-isopropenyl-2-methoxy-4-methylbenzene;
    3. CAS NO:39701-08-1
    4. Molecular Formula: C11H14O
    5. Molecular Weight: 162.232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 39701-08-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 212 °C(Press: 710 Torr)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 0.924±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzene, 2-methoxy-4-methyl-1-(1-methylethenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 2-methoxy-4-methyl-1-(1-methylethenyl)-(39701-08-1)
    11. EPA Substance Registry System: Benzene, 2-methoxy-4-methyl-1-(1-methylethenyl)-(39701-08-1)
  • 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: 39701-08-1(Hazardous Substances Data)

39701-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39701-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,0 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39701-08:
(7*3)+(6*9)+(5*7)+(4*0)+(3*1)+(2*0)+(1*8)=121
121 % 10 = 1
So 39701-08-1 is a valid CAS Registry Number.

39701-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-4-methyl-1-prop-1-en-2-ylbenzene

1.2 Other means of identification

Product number -
Other names 2-(2-Methoxy-4-methylphenyl)prop-1-ene

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:39701-08-1 SDS

39701-08-1Relevant articles and documents

Iridium-Catalyzed C(sp3)?H Addition of Methyl Ethers across Intramolecular Carbon–Carbon Double Bonds Giving 2,3-Dihydrobenzofurans

Ohmura, Toshimichi,Kusaka, Satoshi,Torigoe, Takeru,Suginome, Michinori

, p. 4448 - 4453 (2019/09/16)

Intramolecular addition of an O-methyl C(sp3)?H bond across a carbon-carbon double bond occurs in the iridium-catalyzed reaction of methyl 2-(propen-2-yl)phenyl ethers. The Ir/(S)-DTBM-SEGPHOS catalyst promotes the reaction efficiently in toluene at 110–135 °C to afford 3,3-dimethyl-2,3-dihydrobenzofurans. Enantioselective C(sp3)?H addition is achieved in the reaction of methyl 2-(1-siloxyethenyl)phenyl ethers, affording enantioenriched 3-hydroxy-2,3-dihydrobenzofuran derivatives with up to 96% ee. (Figure presented.).

Lipase-mediated resolution of substituted 2-aryl-propanols: Application to the enantioselective synthesis of phenolic sesquiterpenes

Serra, Stefano

experimental part, p. 619 - 628 (2011/07/08)

A comprehensive study of the lipase-mediated resolution of substituted 2-aryl-propanols is reported. The latter alcohols were submitted to the irreversible acetylation catalyzed either by PPL, CRL, or lipase PS. The enantioselectivity of these transformations was dependent on the type of lipase used. The type of substituents and particularly their position on the aromatic ring strongly affected the selectivity of the reaction. The experiments described prove that PPL is the more versatile lipase catalyzing the acetylation with an enantiomeric ratio (E) value that ranges from 1 up to 144, depending on the substrate used. Conversely, the same transformations were catalyzed by CRL and lipase PS with an enantiomeric ratio value, which is always less than 5. The remarkable behavior of PPL was exploited in the large scale resolution of some substituted 2-aryl-propanols whose enantiomeric forms are relevant building blocks in the enantioselective synthesis of phenolic sesquiterpenes. By these means, the synthesis of (S)-turmeronol B and the formal syntheses of (R)-curcumene, (R)-curcuphenol, (R)-xanthorrhizol, and (R)-curcuhydroquinone were accomplished.

Facile synthesis of (±)-parahigginone methyl ether and (±)-curcuphenol

Du, Zhen-Ting,Li, An-Pai,Peng, Kun,Wu, Tong-Xing,Pan, Xin-Fu

, p. 571 - 574 (2007/10/03)

Using Grinard coupling as a key step, a facile synthetic approach to (±)-parahigginone methyl ether 1 and (±)-curcuphenol 2 has been achieved by five steps with 42.3% and 58.6% overall yield, respectively.

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