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Benzene, 1-bromo-2-(2-bromoethyl)-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 198630-95-4 Structure
  • Basic information

    1. Product Name: Benzene, 1-bromo-2-(2-bromoethyl)-4-methoxy-
    2. Synonyms:
    3. CAS NO:198630-95-4
    4. Molecular Formula: C9H10Br2O
    5. Molecular Weight: 293.986
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 198630-95-4.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: Benzene, 1-bromo-2-(2-bromoethyl)-4-methoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1-bromo-2-(2-bromoethyl)-4-methoxy-(198630-95-4)
    11. EPA Substance Registry System: Benzene, 1-bromo-2-(2-bromoethyl)-4-methoxy-(198630-95-4)
  • 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: 198630-95-4(Hazardous Substances Data)

198630-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 198630-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,6,3 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 198630-95:
(8*1)+(7*9)+(6*8)+(5*6)+(4*3)+(3*0)+(2*9)+(1*5)=184
184 % 10 = 4
So 198630-95-4 is a valid CAS Registry Number.

198630-95-4Relevant articles and documents

Highly diastereoselective synthesis of tetralin-fused spirooxindoles via lewis acid-catalyzed C(sp3)H bond functionalization

Machida, Mizuki,Mori, Keiji

, p. 868 - 871 (2018/07/03)

A highly diastereoselective synthesis of tetralin-fused spirooxindole derivatives was described. Treatment of benzylidene oxindoles with a catalytic amount of Sc(OTf)3 in refluxing hexane afforded the target compounds in good chemical yields with excellent diastereoselectivities (up to >20:1). Detailed investigation of the reaction mechanism revealed that both interconversion of the two diastereomers and their solubility difference in reaction medium were the key to achieving excellent diastereoselectivities.

Regioselective aryl radical cyclisation. Part 2. Synthesis of octahydro-1H-dibenzo[a,d]cycloheptenes through 7-endo ring closure

Ghosh, Ajit K.,Mukhopadhyaya, Jayanta K.,Ghatak, Usha Ranjan

, p. 2747 - 2755 (2007/10/03)

A simple convergent synthesis of trans- and cis-octahydro-1H-dibenzo[a,d]cycloheptenes 15a-c and 16a-c and 20a-c and 21a-c through implementation of a regioselective 7-endo-trig-aryl radical cyclisation of the respective 2-(o-bromoarylethyl)-1-methylenecy

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