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92304-84-2

1,3-(1-2H1)dimethylbenzene, also known as 1,3-dimethyl-2H-benzene, is an organic compound with the molecular formula C8H10. It is a derivative of benzene, where two methyl groups (CH3) are attached to the 1st and 3rd carbon atoms of the benzene ring. 1,3-<(1-2H1)dimethyl>benzene is a colorless liquid with a strong aromatic odor and is used as a chemical intermediate in the synthesis of various organic compounds, such as dyes, pharmaceuticals, and agrochemicals. Due to its chemical structure, 1,3-(1-2H1)dimethylbenzene exhibits properties similar to other alkylbenzenes, such as low reactivity and high thermal stability.

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  • 92304-84-2 Structure

  • Basic information

    1. Product Name: 1,3-<(1-2H1)dimethyl>benzene
    2. Synonyms: 1,3-<(1-2H1)dimethyl>benzene
    3. CAS NO:92304-84-2
    4. Molecular Formula:
    5. Molecular Weight: 107.159
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92304-84-2.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: 1,3-<(1-2H1)dimethyl>benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-<(1-2H1)dimethyl>benzene(92304-84-2)
    11. EPA Substance Registry System: 1,3-<(1-2H1)dimethyl>benzene(92304-84-2)

  • 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: 92304-84-2(Hazardous Substances Data)

92304-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92304-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,0 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92304-84:
(7*9)+(6*2)+(5*3)+(4*0)+(3*4)+(2*8)+(1*4)=122
122 % 10 = 2
So 92304-84-2 is a valid CAS Registry Number.

92304-84-2Relevant articles and documents

Room-Temperature Palladium-Catalyzed Deuterogenolysis of Carbon Oxygen Bonds towards Deuterated Pharmaceuticals

Ou, Wei,Xiang, Xudong,Zou, Ru,Xu, Qing,Loh, Kian Ping,Su, Chenliang

, p. 6357 - 6361 (2021)

Site-specific incorporation of deuterium into drug molecules to study and improve their biological properties is crucial for drug discovery and development. Herein, we describe a palladium-catalyzed room-temperature deuterogenolysis of carbon–oxygen bonds

Method for preparing deuterated compound through decarboxylation and deuteration of carboxylic acid

-

, (2021/06/13)

The invention relates to a method for preparing a deuterated compound through decarboxylation and deuteration of carboxylic acid. According to the method, a carboxylic acid compound is used as a raw material, hydrogen atoms of carboxylate radicals are exc

The Rearrangement of Aromatic Compounds. Part 3. The Mechanism of Rearrangement of Nitrated Hydrocarbons in Trifluoromethanesulphonic Acid

Bullen, John V.,Ridd, John H.,Sabek, Omaima

, p. 1681 - 1685 (2007/10/02)

1,3-Dialkyl-2-nitrobenzenes (C6H3R2NO2; R = Me, Et, and Pri) rearrange in trifluoromethanesulphonic acid to the corresponding 4-nitro derivatives; with R = Et, this reaction is accompanied by dehydration to 7-ethyl-3-methylanthranil.The reaction rate increases markedly with the size of the alkyl group; with R = Me, the reaction was studied at 110 deg C but, with R = Pri, temperatures of 36-54 deg C were used.The studies with R = Me show the reaction to be first-order with the rate coefficients (k1) increasing rapidly with the acidity of the solution 1)/d(-H0)> = 1.45, decreasing with acidity to o.49.Double-labelling experiments with 1H and 15N show the reaction to be intramolecular. 1,2,4-Trimethyl-3-nitrobenzene also rearranges under these conditions to give mainly the 5-nitro isomer.The above results are discussed in terms of a direct 1,3-shift of the nitro group.

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