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C11H11BrO is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446356-77-9 Structure
  • Basic information

    1. Product Name: C11H11BrO
    2. Synonyms:
    3. CAS NO:1446356-77-9
    4. Molecular Formula:
    5. Molecular Weight: 239.112
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446356-77-9.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: C11H11BrO(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H11BrO(1446356-77-9)
    11. EPA Substance Registry System: C11H11BrO(1446356-77-9)
  • 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: 1446356-77-9(Hazardous Substances Data)

1446356-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446356-77-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,3,5 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1446356-77:
(9*1)+(8*4)+(7*4)+(6*6)+(5*3)+(4*5)+(3*6)+(2*7)+(1*7)=179
179 % 10 = 9
So 1446356-77-9 is a valid CAS Registry Number.

1446356-77-9Downstream Products

1446356-77-9Relevant articles and documents

Synthesis of pseudo-indoxyl derivatives via sequential Cu-catalyzed S NAr and Smalley cyclization

Goriya, Yogesh,Ramana, Chepuri V.

, p. 6376 - 6378 (2013)

Ortho-Bromophenyl sec-alkyl/sec-alkenyl ketones, on reaction with sodium azide in the presence of copper salts, undergo sequential SNAr followed by Smalley cyclization to provide pseudo-indoxyl derivatives. Some of these pseudo-indoxyl derivati

Phosphine-Catalyzed Intramolecular Vinylogous Aldol Reaction of α-Substituted Enones

Mondal, Atanu,Satpathi, Bishnupada,Ramasastry

, p. 256 - 261 (2022/01/04)

We demonstrate the first phosphine-catalyzed intramolecular vinylogous aldol reaction (IVAR) of α-substituted enones. This strategy provides access to various pentannulated (hetero)arenes and dibenzocycloheptanones incorporated with two contiguous stereocenters, one of which is an all-carbon quaternary center. The scope of this work is further broadened through elaborations of the IVAR adducts to (i) benzannulated nine-membered carbocyclic systems, (ii) interesting classes of 1,3-dienes, 1,3,5-trienes, and 1-yn-3,5-dienes, and (iii) the analogs of echinolactone D and russujaponol F.

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