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Benzene, 1,1'-(2-methylpropylidene)bis[2,4-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85238-99-9 Structure
  • Basic information

    1. Product Name: Benzene, 1,1'-(2-methylpropylidene)bis[2,4-dimethoxy-
    2. Synonyms:
    3. CAS NO:85238-99-9
    4. Molecular Formula: C20H26O4
    5. Molecular Weight: 330.424
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85238-99-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzene, 1,1'-(2-methylpropylidene)bis[2,4-dimethoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1,1'-(2-methylpropylidene)bis[2,4-dimethoxy-(85238-99-9)
    11. EPA Substance Registry System: Benzene, 1,1'-(2-methylpropylidene)bis[2,4-dimethoxy-(85238-99-9)
  • 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: 85238-99-9(Hazardous Substances Data)

85238-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85238-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,3 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85238-99:
(7*8)+(6*5)+(5*2)+(4*3)+(3*8)+(2*9)+(1*9)=159
159 % 10 = 9
So 85238-99-9 is a valid CAS Registry Number.

85238-99-9SDS

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-[1-(2,4-dimethoxyphenyl)-2-methylpropyl]-2,4-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names 1,1-bis(2,4-dimethoxyphenyl)-2-methylpropane

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:85238-99-9 SDS

85238-99-9Relevant articles and documents

Novel and highly efficient one pot protocol for the synthesis of diversely functionalized triarylmethanes

Babu, B. Madhu,Thakur, Pramod B.,Bangade, Vikas M.,Meshram

supporting information, p. 766 - 771 (2015/02/19)

An efficient, convenient, and novel one pot approach is described for the synthesis of triarylmethanes by in situ oxidation of benzylalcohols followed by the Friedel-Crafts alkylation of di/trimethoxybenzenes in the presence of BF3·OEt2. The generality of the present method is strengthened by screening a variety of aromatic, aliphatic, and heteroaromatic alcohols with methoxy arenes. Shorter reaction time, mild reaction condition, good yields, and wide scope of substrates are the significant features of this protocol.

Dimethoxy aromatic compounds VIII. Degenerate dealkylation-realkylation reaction of 1-bis(2,4-dimethoxyphenyl)-2-methylpropane

Natoli,Ceraulo,Lamartina,Ferrugia

, p. 375 - 376 (2007/10/02)

The condensation reaction under acid condition of the benzylic alcohols 1, 2 and 3 with the hexadeutero dimethoxybenzenes 4, 5 and 6 leads to the expected hexadeutero bis(dimethoxyphenyl)-2-methylpropanes 7, 8 and 9, respectively. However, the presence of both dodecadeutero and unlabelled 1- bis(2,4-dimethoxyphenyl)-2-methylpropanes 10 and 11 indicates that 9 undergoes a rapid degenerate dealkylation-alkylation reaction.

DIMETHOXY AROMATIC COMPOUNDS. I. ACID-CATALYZED CONDENSATION OF 1,3-DIMETHOXYBENZENE WITH ISOBUTYRALDEHYDE

Natoli, Maria C.,Agozzino, Pasquale,Ceraulo, Leopoldo,Lamartina, Liliana

, p. 403 - 408 (2007/10/02)

The title reaction involves exclusively 4- and 6-positions of 1,3-dimethoxybenzene.The main reaction products, including some oligomers, were chromatographically isolated and characterized by 1H- and 13C-NMR, and mass spectra.

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