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4,5-Dimethylbenzene-1,2-dimethanol, also known as 4,5-dimethyl-1,2-benzenedimethanol, is a chemical compound that belongs to the family of aromatic alcohols. These are compounds that contain a benzene ring with at least one hydrogen atom replaced by a hydroxy group. It is composed of multiple methyl and hydroxyl groups attached to a benzene ring, resulting in a molecular formula of C10H14O2. However, information about its usage, synthesis, properties, and effects on the environment or human health is quite limited. The safety data, handling precautions, or potential applications are also not well documented, which necessitates cautious usage due to potential unpredictable effects.

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  • 60070-05-5 Structure
  • Basic information

    1. Product Name: 4,5-DIMETHYLBENZENE-1,2-DIMETHANOL
    2. Synonyms: 4,5-DIMETHYLBENZENE-1,2-DIMETHANOL;4,5-Dimethylbenzene-1,2-dimethanlol
    3. CAS NO:60070-05-5
    4. Molecular Formula: C10H14O2
    5. Molecular Weight: 166.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 60070-05-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 320.2 °C at 760 mmHg
    3. Flash Point: 156.4 °C
    4. Appearance: /
    5. Density: 1.11 g/cm3
    6. Vapor Pressure: 0.000134mmHg at 25°C
    7. Refractive Index: 1.566
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4,5-DIMETHYLBENZENE-1,2-DIMETHANOL(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4,5-DIMETHYLBENZENE-1,2-DIMETHANOL(60070-05-5)
    12. EPA Substance Registry System: 4,5-DIMETHYLBENZENE-1,2-DIMETHANOL(60070-05-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 24/25
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 60070-05-5(Hazardous Substances Data)

60070-05-5 Usage

Uses

Due to the limited information available on 4,5-dimethylbenzene-1,2-dimethanol, its applications are not well-defined. However, based on its chemical structure and the properties of similar compounds, it can be inferred that it may have potential uses in various industries. These applications could include:
Used in Chemical Synthesis:
4,5-Dimethylbenzene-1,2-dimethanol could be used as a building block or intermediate in the synthesis of more complex organic compounds, such as pharmaceuticals, agrochemicals, or specialty chemicals. Its presence of multiple functional groups, including hydroxyl and methyl groups, may facilitate reactions that lead to the formation of desired products.
Used in Material Science:
4,5-DIMETHYLBENZENE-1,2-DIMETHANOL may also have potential applications in the development of new materials, such as polymers or coatings, due to its aromatic structure and functional groups. The hydroxyl groups could potentially participate in condensation reactions to form polymers, while the methyl groups may contribute to the overall stability and properties of the material.
Used in Research and Development:
4,5-Dimethylbenzene-1,2-dimethanol could be utilized in academic or industrial research settings to study its properties, reactivity, and potential applications. Researchers may investigate its behavior in various chemical reactions or explore its use in novel synthesis pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 60070-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,7 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60070-05:
(7*6)+(6*0)+(5*0)+(4*7)+(3*0)+(2*0)+(1*5)=75
75 % 10 = 5
So 60070-05-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2/c1-7-3-9(5-11)10(6-12)4-8(7)2/h3-4,11-12H,5-6H2,1-2H3

60070-05-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-Dimethylbenzene-1,2-Dimethanol

1.2 Other means of identification

Product number -
Other names [2-(hydroxymethyl)-4,5-dimethylphenyl]methanol

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:60070-05-5 SDS

60070-05-5Relevant articles and documents

A Unified Catalytic Asymmetric (4+1) and (5+1) Annulation Strategy to Access Chiral Spirooxindole-Fused Oxacycles

Gao, Min,Gong, Xiangnan,Hu, Lin,Luo, Yanshu,Xia, Yuanzhi,Xu, Qianlan,Zhao, Yukun

supporting information, p. 19813 - 19820 (2021/08/03)

A unified catalytic asymmetric (N+1) (N=4, 5) annulation reaction of oxindoles with bifunctional peroxides has been achieved in the presence of a chiral phase-transfer catalyst (PTC). This general strategy utilizes peroxides as unique bielectrophilic four- or five-atom synthons to participate in the C?C and the subsequent umpolung C?O bond-forming reactions with one-carbon unit nucleophiles, thus providing a distinct method to access the valuable chiral spirooxindole-tetrahydrofurans and -tetrahydropyrans with good yields and high enantioselectivities under mild conditions. DFT calculations were performed to rationalize the origin of high enantioselectivity. The gram-scale syntheses and synthetic utility of the resultant products were also demonstrated.

Methyl and Dimethyl o-Xylenyl-Substituted Fullerene Acceptors for Polymer Solar Cells

Kim, Hee Un,Park, Jong Baek,Grimsdale, Andrew C.,Hwang, Do-Hoon

, p. 1017 - 1027 (2015/09/28)

A series of fullerene derivatives based on methyl- and dimethyl-substituted o-xylenyl groups were synthesized via Diels-Alder reaction from fullerene (C60) and dienes derived from α,α′-dibromo-o-xylene derivatives. The synthesized 1-methyl-4,5-

Closely stacked oligo(phenylene ethynylene)s: Effect of π-stacking on the electronic properties of conjugated chromophores

Jagtap, Subodh P.,Mukhopadhyay, Sukrit,Coropceanu, Veaceslav,Brizius, Glen L.,Bredas, Jean-Luc,Collard, David M.

supporting information; experimental part, p. 7176 - 7185 (2012/06/15)

In this work, a bicyclo[4.4.1]undecane scaffold is used to hold oligo(phenylene ethynylene) units in a cofacially stacked arrangement along the entire length of the conjugated units. We study the impact that the resulting strong interchain interactions ha

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