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1254703-41-7

(1R,2R)-[2-(p-toluidino)-1,2-dihydronaphthalen-1-yl]carbamic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1254703-41-7 Structure

  • Basic information

    1. Product Name: (1R,2R)-[2-(p-toluidino)-1,2-dihydronaphthalen-1-yl]carbamic acid tert-butyl ester
    2. Synonyms:
    3. CAS NO:1254703-41-7
    4. Molecular Formula:
    5. Molecular Weight: 350.461
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1254703-41-7.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: (1R,2R)-[2-(p-toluidino)-1,2-dihydronaphthalen-1-yl]carbamic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2R)-[2-(p-toluidino)-1,2-dihydronaphthalen-1-yl]carbamic acid tert-butyl ester(1254703-41-7)
    11. EPA Substance Registry System: (1R,2R)-[2-(p-toluidino)-1,2-dihydronaphthalen-1-yl]carbamic acid tert-butyl ester(1254703-41-7)

  • 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: 1254703-41-7(Hazardous Substances Data)

1254703-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1254703-41-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,7,0 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1254703-41:
(9*1)+(8*2)+(7*5)+(6*4)+(5*7)+(4*0)+(3*3)+(2*4)+(1*1)=137
137 % 10 = 7
So 1254703-41-7 is a valid CAS Registry Number.

1254703-41-7Downstream Products

1254703-41-7Relevant articles and documents

Iridium-catalyzed asymmetric ring opening of azabicyclic alkenes by amines

Long, Yuhua,Yang, Dingqiao,Zhang, Zhenming,Wu, Yujuan,Zeng, Heping,Chen, Yu

experimental part, p. 7291 - 7299 (2011/01/12)

The enantioselective ring-opening reactions of azabicyclic alkenes with primary and secondary aromatic amine nucleophiles are reported using an iridium catalyst generated in situ from 1.5 mol % of [Ir(COD)Cl]2 and 3 mol % of (S)-BINAP. The reac

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