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CAS

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1335455-01-0

N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1335455-01-0 Structure

  • Basic information

    1. Product Name: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine
    2. Synonyms: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine
    3. CAS NO:1335455-01-0
    4. Molecular Formula:
    5. Molecular Weight: 364.271
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1335455-01-0.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: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine(1335455-01-0)
    11. EPA Substance Registry System: N-(tert-butyl)-2,5-bis(4-chlorophenyl)-1,3-dioxol-4-amine(1335455-01-0)

  • 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: 1335455-01-0(Hazardous Substances Data)

1335455-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1335455-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,4,5 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1335455-01:
(9*1)+(8*3)+(7*3)+(6*5)+(5*4)+(4*5)+(3*5)+(2*0)+(1*1)=140
140 % 10 = 0
So 1335455-01-0 is a valid CAS Registry Number.

1335455-01-0Downstream Products

1335455-01-0Relevant articles and documents

A [bmim]Cl-promoted domino protocol using an isocyanide-based [4+1]-cycloaddition reaction for the synthesis of diversely functionalized 3-Alkylamino-2-Alkyl/aryl/hetero-Aryl indolizine-1-carbonitriles under solvent-free conditions

Jadhav, Arvind H.,Atar, Amol Balu,Kang, Jongmin

, p. 3241 - 3248 (2020)

A domino protocol involving aldehydes, isocyanides and 2-pyridylacetonitrile in the presence of [bmim]Cl as a promoter and solvent for the synthesis of 3-Alkylamino-2-Alkyl/arylindolizine-1-carbonitriles is described. A wide range of alkyl, aryl and heter

SiO2Nanoparticle-catalyzed Facile and Efficient One-pot Synthesis of N-alkyl-2,5-bis[(E)-2-phenylvinyl]-1,3-dioxol-4-amine Under Solvent-free Conditions

Bayat, Mohammad,Nasehfard, Hamideh

, p. 1474 - 1478 (2016/09/23)

1,3-Dioxole-4-amine derivatives have been prepared efficiently in one-pot reaction using nanosized SiO2as a heterogeneous catalyst. The present method does not involve any hazardous organic solvents or catalysts. The high surface-to-volume rati

A simple one-pot synthesis of N-alkyl-2,5-diaryl-1,3-dioxol-4-amines

Bayat, Mohammad,Nasri, Shima

experimental part, p. 1657 - 1661 (2011/11/01)

An efficient procedure for the synthesis of N-alkyl-2,5-diaryl-1,3-dioxol- 4-amines 3 via a one-pot reaction of aromatic aldehydes 2 and alkyl isocyanides 1 at room temperature in good yields is described (Scheme 1, Table). Copyright

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