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Methyl 2-methylbiphenyl-4-carboxylate is an ester class organic compound with a fruity, floral odor and a sweet, jasmine-like aroma. It is commonly used as a fragrance ingredient in perfumes and other scented products, and also has potential applications in pharmaceuticals and agrochemicals.

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  • 892843-59-3 Structure
  • Basic information

    1. Product Name: Methyl 2-methylbiphenyl-4-carboxylate
    2. Synonyms: Methyl 2-methylbiphenyl-4-carboxylate
    3. CAS NO:892843-59-3
    4. Molecular Formula: C15H14O2
    5. Molecular Weight: 226.27046
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 892843-59-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 2-methylbiphenyl-4-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 2-methylbiphenyl-4-carboxylate(892843-59-3)
    11. EPA Substance Registry System: Methyl 2-methylbiphenyl-4-carboxylate(892843-59-3)
  • 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: 892843-59-3(Hazardous Substances Data)

892843-59-3 Usage

Uses

Used in Fragrance Industry:
Methyl 2-methylbiphenyl-4-carboxylate is used as a fragrance ingredient for its fruity, floral, and sweet jasmine-like aroma, adding a pleasant scent to perfumes and other scented products.
Used in Pharmaceutical Industry:
Methyl 2-methylbiphenyl-4-carboxylate is used as a potential pharmaceutical ingredient due to its chemical properties and potential applications in the development of new drugs.
Used in Agrochemical Industry:
Methyl 2-methylbiphenyl-4-carboxylate is used as a potential ingredient in agrochemicals, contributing to the development of new products for agricultural applications.

Check Digit Verification of cas no

The CAS Registry Mumber 892843-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,2,8,4 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 892843-59:
(8*8)+(7*9)+(6*2)+(5*8)+(4*4)+(3*3)+(2*5)+(1*9)=223
223 % 10 = 3
So 892843-59-3 is a valid CAS Registry Number.

892843-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-methyl-4-phenylbenzoate

1.2 Other means of identification

Product number -
Other names methyl 4-phenyl-3-methylbenzoate

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:892843-59-3 SDS

892843-59-3Relevant articles and documents

Palladium-Catalyzed Alkynylation of Morita-Baylis-Hillman Carbonates with (Triisopropylsilyl)acetylene on Water

Li, Yangxiong,Liu, Li,Kong, Delong,Wang, Dong,Feng, Weichun,Yue, Tao,Li, Chaojun

, p. 6283 - 6290 (2015/06/30)

Direct alkynylation of Morita-Baylis-Hillman carbonates with (triisopropylsilyl)acetylene catalyzed by a Pd(OAc)2-NHC complex was developed "on water" to give the corresponding 1,4-enynes. The significant effects of water amount in the solvent

ANTIPROLIFERATIVE BENZO [B] AZEPIN- 2 - ONES

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Page/Page column 49, (2014/02/15)

Disclosed are compounds of Formula (I) or pharmaceutically acceptable salts thereof, wherein W, X, Y, Z, R1, R2, R3 and R4 are described in this application, and methods of using said compounds in the treatment of cancer.

Design, synthesis and identification of novel colchicine-derived immunosuppressant

Chang, Dong-Jo,Yoon, Eun-Young,Lee, Geon-Bong,Kim, Soon-Ok,Kim, Wan-Joo,Kim, Young-Myeong,Jung, Jong-Wha,An, Hongchan,Suh, Young-Ger

scheme or table, p. 4416 - 4420 (2010/04/05)

Synthesis and biological evaluation of various colchicine analogues through the mixed-lymphocyte reaction (MLR), lymphoproliferation, and inhibitory effects on the inflammatory genes are described. In addition, a new series of immunosuppressive agents developed on the structural basis of colchicine, as well as their structure-activity relationships is reported. The most potent analogue 20a exhibited an excellent immunosuppressive activity on in vivo skin-allograft model, which is comparable to that of cyclosporin A.

AMINO ACID COMPOUNDS

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Page/Page column 45-46, (2009/12/23)

[Problem] To provide novel compounds that are S1P1 receptor agonists and exhibit an immunosuppressive activities by inducing lymphocyte sequestration in secondary lymphoid tissues. In addition, to provide a pharmaceutical agent which comprises the compounds as an effective component, in particular to provide a therapeutic and/or prophylactic agent for an autoimmune disease and the like. [Solving Means] Amino acid compounds that are represented by the following Formula (1) are provided

NOVEL MCH RECEPTOR ANTAGONISTS

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Page/Page column 105-106, (2008/06/13)

The present invention relates to a melanin concentrating hormone antagonist compound of formula (I); wherein Ar1, L1, R1, q, X, R2, R3, R4, and R5 are as defined, or a pharmaceutically acceptable salt, solvate, or enantiomer thereof useful in the treatment, prevention or amelioration of symptoms associated with obesity and related diseases.

Recent progress on the iterative construction of 4-substituted-3-hydroxy benzoic acids from unsaturated aldehydes and dimethyl succinate

Brenna, Elisabetta,Fuganti, Claudio,Perozzo, Valentina,Serra, Stefano

, p. 15029 - 15040 (2007/10/03)

An improvement of a known two step cyclization procedure, affording 4-aryl-3-hydroxy benzoic acid derivatives from 3-aryl-2,3-unsaturated aldehydes and dimethyl succinate, is described. The high versatility of the synthetic procedure is shown, as the aryl substituent can be a benzene or naphthalene moiety, or an heteroaromatic ring. It can be applied iteratively to prepare p,p'-oligophenyl derivatives.

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