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CAS

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882747-46-8

methyl 4-romo--phenylsulfonyl)H-yrrole--arboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 882747-46-8 Structure

  • Basic information

    1. Product Name: methyl 4-romo--phenylsulfonyl)H-yrrole--arboxylate
    2. Synonyms: methyl 4-romo--phenylsulfonyl)H-yrrole--arboxylate
    3. CAS NO:882747-46-8
    4. Molecular Formula:
    5. Molecular Weight: 344.186
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 882747-46-8.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: methyl 4-romo--phenylsulfonyl)H-yrrole--arboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-romo--phenylsulfonyl)H-yrrole--arboxylate(882747-46-8)
    11. EPA Substance Registry System: methyl 4-romo--phenylsulfonyl)H-yrrole--arboxylate(882747-46-8)

  • 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: 882747-46-8(Hazardous Substances Data)

882747-46-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 882747-46-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,7,4 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 882747-46:
(8*8)+(7*8)+(6*2)+(5*7)+(4*4)+(3*7)+(2*4)+(1*6)=218
218 % 10 = 8
So 882747-46-8 is a valid CAS Registry Number.

882747-46-8Relevant articles and documents

Optional synthesis of 2- OR 5-substituted 3-bromopyrroles via bromine-lithium exchange of N-benzenesulfonyl-2,4-dibromopyrrole

Fukuda, Tsutomu,Iwao, Masatomo

, p. 1261 - 1273 (2013/08/23)

The regioselective bromine-lithium exchange of N-benzenesulfonyl-2,4- dibromopyrrole (6) with n-BuLi followed by treatment with various electrophiles gave 5-substituted 3-bromopyrroles (5) in excellent yields. In contrast, the sequential treatment of 6 wi

Directed lithiation of N -benzenesulfonyl-3-bromopyrrole. Electrophile-controlled regioselective functionalization via dynamic equilibrium between C-2 and C-5 lithio species

Fukuda, Tsutomu,Ohta, Takeshi,Sudo, Ei-Ichi,Iwao, Masatomo

supporting information; experimental part, p. 2734 - 2737 (2010/08/19)

(Figure presented) Directed lithiation of N-benzenesulfonyl-3-bromopyrrole (1) with LDA in THF at -78 °C generated C-2 lithio species 3 selectively. Reactions of 3 with reactive electrophiles produced the corresponding 2-functionalized pyrroles 4. On the

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