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2-Hydroxy-6-methyl-4-(phenylmethoxy)benzoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22375-05-9 Structure
  • Basic information

    1. Product Name: 2-Hydroxy-6-methyl-4-(phenylmethoxy)benzoic acid methyl ester
    2. Synonyms: 2-Hydroxy-6-methyl-4-(phenylmethoxy)benzoic acid methyl ester
    3. CAS NO:22375-05-9
    4. Molecular Formula: C16H16O4
    5. Molecular Weight: 272.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22375-05-9.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: 2-Hydroxy-6-methyl-4-(phenylmethoxy)benzoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Hydroxy-6-methyl-4-(phenylmethoxy)benzoic acid methyl ester(22375-05-9)
    11. EPA Substance Registry System: 2-Hydroxy-6-methyl-4-(phenylmethoxy)benzoic acid methyl ester(22375-05-9)
  • 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: 22375-05-9(Hazardous Substances Data)

22375-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22375-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,7 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22375-05:
(7*2)+(6*2)+(5*3)+(4*7)+(3*5)+(2*0)+(1*5)=89
89 % 10 = 9
So 22375-05-9 is a valid CAS Registry Number.

22375-05-9SDS

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 methyl 2-hydroxy-6-methyl-4-phenylmethoxybenzoate

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-6-methyl-4-(phenylmethoxy)benzoic acid methyl ester

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:22375-05-9 SDS

22375-05-9Relevant articles and documents

Photolytic Studies on the Generation and Trapping of 6-Oxomethylidenecyclohexa-2,4-diene-1-one Derivatives with Various Nucleophiles

Mies, Thomas,White, Andrew J. P.,Parsons, Philip J.,Barrett, Anthony G. M.

, (2021/11/17)

α-Oxoketenes and cyclohexadiene α-oxoketenes are reactive intermediates, particularly the latter due to their high re-aromatization potential. In this communication, we report photolytic studies on the generation of such species from 4-OMe and 4-OMOM protected resorcylate dioxinones and their trapping to give resorcylate esters and amides as well as the formation of adducts with enol-ethers as trapping reagents.

First Total Synthesis of (3 R,4 S)-4-Hydroxylasiodiplodin: A Facile and Stereoselective Approach

Bujaranipalli, Sheshurao,Eppa, Gyan Chander,Das, Saibal

, p. 1117 - 1120 (2013/06/27)

A first total synthesis of (3R,4S)-4-hydroxylasiodiplodin is described starting from methyl acetoacetate and a commonly available carbohydrate, d-mannitol, which is regularly used in organic synthesis. The facile and stereoselective approach involves the

SYNTHESES OF 4-HYDROXY-5-IODO-2,3-DIMETHOXY-6-METHYLBENZOIC ACID AND 5-BROMO-4-HYDROXY-2,3-DIMETHOXY-6-METHYLBENZOIC ACID - AROMATIC CONSTITUENTS OF THE CALICHEMICINS

Laak, Kai van,Scharf, Hans-Dieter

, p. 5511 - 5516 (2007/10/02)

4-Hydroxy-5-iodo-2,3-dimethoxy-6-methylbenzoic acid (1) and 5-bromo-4-hydroxy-2,3-dimethoxy-6-methylbenzoic acid (2) are the polysubstituted aromatic carboxylic acids found in calichemicin antibiotics.The title compounds are synthesized on preparative sca

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

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