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N-benzyloxycarbonyl-3-phenyl-1-(thien-2-yl)-prop-2-yn-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1379681-76-1 Structure
  • Basic information

    1. Product Name: N-benzyloxycarbonyl-3-phenyl-1-(thien-2-yl)-prop-2-yn-1-amine
    2. Synonyms:
    3. CAS NO:1379681-76-1
    4. Molecular Formula:
    5. Molecular Weight: 347.437
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1379681-76-1.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: N-benzyloxycarbonyl-3-phenyl-1-(thien-2-yl)-prop-2-yn-1-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyloxycarbonyl-3-phenyl-1-(thien-2-yl)-prop-2-yn-1-amine(1379681-76-1)
    11. EPA Substance Registry System: N-benzyloxycarbonyl-3-phenyl-1-(thien-2-yl)-prop-2-yn-1-amine(1379681-76-1)
  • 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: 1379681-76-1(Hazardous Substances Data)

1379681-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379681-76-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,6,8 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1379681-76:
(9*1)+(8*3)+(7*7)+(6*9)+(5*6)+(4*8)+(3*1)+(2*7)+(1*6)=221
221 % 10 = 1
So 1379681-76-1 is a valid CAS Registry Number.

1379681-76-1Downstream Products

1379681-76-1Relevant articles and documents

Enantioselective zinc/BINOL-catalysed alkynylation of aldimines generated in situ from α-amido sulfones

Blay, Gonzalo,Brines, Ana,Monleon, Alicia,Pedro, Jose R.

supporting information; experimental part, p. 2440 - 2444 (2012/03/26)

Chiral nonracemic N-Cbz-protected propargylic amines have been prepared by the addition of terminal alkynes to imines generated in situ from α-amido sulfones in the presence of diethylzinc and BINOL-type ligands as catalysts. The reactions give good yields and high enantioselectivities (ee values up to 95 %) for a good number of aromatic and heteroaromatic α-amido sulfones and alkynes. Copyright

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