Welcome to LookChem.com Sign In|Join Free

CAS

  • or

215648-56-9

2-(Chlorosulfonyl)-3-methoxybenzoic acid methyl ester is a chemical compound with the formula C9H9ClO5S. It is a methyl ester of 2-(chlorosulfonyl)-3-methoxybenzoic acid, characterized by its strong and reactive chlorosulfonyl group. This white to light brown solid is soluble in organic solvents such as methanol and acetone, and is widely recognized for its versatile reactivity and usefulness as a building block in organic synthesis.

215648-56-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 215648-56-9 Structure

  • Basic information

    1. Product Name: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER
    2. Synonyms: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER
    3. CAS NO:215648-56-9
    4. Molecular Formula: C9H9ClO5S
    5. Molecular Weight: 264.68
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 215648-56-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 394.0±32.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.407±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER(215648-56-9)
    11. EPA Substance Registry System: 2-(CHLOROSULFONYL)-3-METHOXYBENZOIC ACID METHYL ESTER(215648-56-9)

  • 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: 215648-56-9(Hazardous Substances Data)

215648-56-9 Usage

Uses

Used in Pharmaceutical Industry:
2-(Chlorosulfonyl)-3-methoxybenzoic acid methyl ester is used as an intermediate in the production of pharmaceuticals for its ability to facilitate the synthesis of various drug compounds. Its strong chlorosulfonyl group aids in chemical transformations, making it a valuable component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(Chlorosulfonyl)-3-methoxybenzoic acid methyl ester serves as an intermediate in the synthesis of agrochemicals, contributing to the creation of effective pesticides and other agricultural products. Its reactivity allows for the production of compounds that can protect crops and enhance agricultural yields.
Used in Research and Development:
2-(Chlorosulfonyl)-3-methoxybenzoic acid methyl ester is utilized in research and development settings as a key compound for exploring new chemical reactions and syntheses. Its potential applications in advancing scientific knowledge and developing innovative products make it an important tool in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 215648-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,6,4 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 215648-56:
(8*2)+(7*1)+(6*5)+(5*6)+(4*4)+(3*8)+(2*5)+(1*6)=139
139 % 10 = 9
So 215648-56-9 is a valid CAS Registry Number.

215648-56-9Downstream Products

215648-56-9Relevant articles and documents

Substituted sulphonylamino(thio)carbonyl compounds as herbicides

-

, (2008/06/13)

The invention relates to novel substituted sulphonylamino(thio)carbonyl compounds of the formula (I) in whichA represents oxygen, sulphur, NH, N-alkyl, N-aryl, —CH=N—, or —N=CH—or —CH=CH—,Q represents oxygen or sulphur,R1 represents respectively optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, heterocyclyl or heterocyclylalkyl,R2 represents cyano, nitro, halogen or represents respectively optionally substituted alkyl, alkoxy, alkoxycarbonyl, alkylthio, alkylsulphinyl, alkylsulphonyl, alkenyl, alkinyl, alkenyloxy or alkinyloxy, andR3 represents respectively optionally substituted heterocyclyl having 5 ring members of which at least one represents oxygen, sulphur or nitrogen and a further one to three may represent nitrogen,(except for certain individual prior art compounds), furthermore to salts of novel compounds of the formula (I), to various processes and novel intermediates for preparing the novel compounds and to their use as herbicides.

N-(?1, 2, 4! triazoloazinyl) benzenesulfonamide and pyridinesulfonamide compounds and their use as herbicides

-

, (2008/06/13)

N-(Triazoloazinyl)arylsulfonamide compounds, such as 2,6-dimethoxy-N-(8-chloro-5-methoxy?1,2,4!-triazolo?1,5-c!pyrimidin-2-yl)benzenesulfonamide, 2-methoxy-4-(trifluoromethyl)-N-(5,8-dimethoxy?1,2,4!-triazolo?1,5-c!pyrimidin-2-yl)pyridine-3-sulfonamide, a

Endothelin receptor antagonists: Synthesis and structure-activity relationships of substituted benzothiazine-1,1-dioxides

Berryman,Edmunds,Bunker,Haleen,Bryant,Welch,Doherty

, p. 1447 - 1456 (2007/10/03)

The development of benzothiazine-1,1-dioxide derivatives as a new structural class of potent endothelin receptor antagonists is described. Structure-activity relationships (SAR) revealed that PD164800 (1) is a potent antagonist of the ET(A) receptor subtype. Copyright (C) 1998 Elsevier Science Ltd.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 215648-56-9