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1316826-08-0

C14H13BrSe is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1316826-08-0 Structure

  • Basic information

    1. Product Name: C14H13BrSe
    2. Synonyms:
    3. CAS NO:1316826-08-0
    4. Molecular Formula:
    5. Molecular Weight: 340.121
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1316826-08-0.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: C14H13BrSe(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H13BrSe(1316826-08-0)
    11. EPA Substance Registry System: C14H13BrSe(1316826-08-0)

  • 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: 1316826-08-0(Hazardous Substances Data)

1316826-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1316826-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,6,8,2 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1316826-08:
(9*1)+(8*3)+(7*1)+(6*6)+(5*8)+(4*2)+(3*6)+(2*0)+(1*8)=150
150 % 10 = 0
So 1316826-08-0 is a valid CAS Registry Number.

1316826-08-0Relevant articles and documents

Efficient and highly selective method for the synthesis of 4-Iodo-3-substituted 1 H -Isoselenochromenes and -isothiochromenes

Schneider, Caroline C.,Bortolatto, Cristiani,Back, Davi F.,Menezes, Paulo H.,Zeni, Gilson

, p. 413 - 418 (2011)

We present here our results on the preparation of 2-alkynylbenzyl selenide and sulfide derivatives via Sonogashira cross-coupling of benzyl chalcogenides with different alkynes. This cross-coupling reaction proceeded cleanly under mild conditions and was performed with propargyl alcohol as well as alkyl- and arylalkynes. Subsequent electrophilic-cyclization reaction of the 2-alkynylbenzyl selenide and sulfide derivatives using iodine as an electrophilic source gave 4-iodo-3-substituted 1H-isoselenochromenes and -isothiochromenes in moderate yields. The unique product obtained during the course of this cyclization contained a six-membered ring which was confirmed by X-ray diffraction analysis. Georg Thieme Verlag Stuttgart - New York.

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