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3465-63-2

4-Hydroxy-2-methoxy-6-methylbenzoic acid methyl ester is an organic compound with the chemical formula C10H12O5. It is a derivative of benzoic acid, featuring a hydroxyl group at the 4-position, a methoxy group at the 2-position, and a methyl group at the 6-position. The methyl ester functional group is attached to the carboxylic acid group, making it a methyl ester of the parent benzoic acid. 4-Hydroxy-2-methoxy-6-methylbenzoic acid methyl ester is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through chemical reactions involving benzoic acid derivatives and is used as an intermediate in the production of more complex molecules.

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  • 3465-63-2 Structure

  • Basic information

    1. Product Name: 4-Hydroxy-2-methoxy-6-methylbenzoic acid methyl ester
    2. Synonyms: 4-Hydroxy-2-methoxy-6-methylbenzoic acid methyl ester
    3. CAS NO:3465-63-2
    4. Molecular Formula: C10H12O4
    5. Molecular Weight: 196.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3465-63-2.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: 4-Hydroxy-2-methoxy-6-methylbenzoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Hydroxy-2-methoxy-6-methylbenzoic acid methyl ester(3465-63-2)
    11. EPA Substance Registry System: 4-Hydroxy-2-methoxy-6-methylbenzoic acid methyl ester(3465-63-2)

  • 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: 3465-63-2(Hazardous Substances Data)

3465-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3465-63-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3465-63:
(6*3)+(5*4)+(4*6)+(3*5)+(2*6)+(1*3)=92
92 % 10 = 2
So 3465-63-2 is a valid CAS Registry Number.

3465-63-2SDS

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 methyl 4-hydroxy-2-methoxy-6-methylbenzoate

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-2-methoxy-6-methyl-benzoesaeure-methylester

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:3465-63-2 SDS

3465-63-2Relevant articles and documents

Two new glycosides from Dianella ensifolia (L.) DC

Fan, Miao-Yin,Liu, Bing-Rui,Yang, Fan,Zhang, Pu-Zhao

, p. 18 - 20 (2021/11/11)

The Dianella genus includes approximately 20 species in all over the world. So far, only the chemical constituents of the lipophilic extract from Dianella ensifolia have been investigated. However, there have been no reports of its aqueous extract. In thi

WAVELENGTH DEPENDENT PHOTOISOMERIZATION OF BICYCLOHEXENONES

Dauben, William G.,Cogen, Jeffrey M.,Behar, Victor,Schultz, Arthur G.,Geiss, William,Taveras, Arthur G.

, p. 1713 - 1716 (2007/10/02)

The unusual wavelength dependent product selectivity observed upon irradiation of a substituted 2,5-cyclohexadien-1-one is shown to result from wavelength dependent quantum yields for rearreangement of the primary photoproduct bicyclohexenones.Reaction selectivity can be optimized by careful choice of irradiation wavelength and length of irradiation time.

Improved Synthesis of Dichloroisoeverninic Acid

Dornhagen, Juergen,Scharf, Hans-Dieter

, p. 1541 - 1549 (2007/10/02)

The Dichlorination of methyl isoeverninate 7a gave the geminal dichloroketone 12 as the major product.The title compound 1 was therefore synthesized via dichlorination of 4-protected methyl orsellinate 5a using the pivaloyloxy-function as a new protecting group in resorcyclic acids chemistry. - Keywords: 3,5-Dichloro-4-hydroxy-2-methoxy-6-methylbenzoic Acid, Dichloroisoeverninic Acid

2,3-Alkadiensaeureester als Dienophile; Anwendung bei der Synthese von (+)-(R)-Lasiodiplodin

Fink, Margot,Gaier, Hans,Gerlach, Hans

, p. 2563 - 2569 (2007/10/02)

Methyl 2,3-alkadienoates 2 are shown to react at 80 deg C with 1,1-dimethoxy-3-trimethylsilyloxy-1,3-butadiene (1) to give the adducts 3 in good yields.Rearrangement of 3, catalyzed by p-toluenesulfonic acid or by sodium methoxide, affords the 6-substitut

2'-O-Methyltenuiorin, 2"-O-Methyltenuiorin and 2',2"-Di-O-methyltenuiorin. Three News Tridepsides from the Lichen Pseudocyphellaria faveolata

Elix, John A.,Lajide, Labunmi

, p. 2005 - 2011 (2007/10/02)

The tridepsides 2'-O-methyltenuiorin, 2"-O-methyltenuiorin and 2',2"-di-O-methyltenuiorin have been isolated from the lichen Pseudocyphellaria faveolata in addition to the well known compounds tenuiorin, physciosporin and sticnic acid.The structure of the

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