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69982-05-4

2-Thiazolamine, N-(triphenylphosphoranylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69982-05-4 Structure

  • Basic information

    1. Product Name: 2-Thiazolamine, N-(triphenylphosphoranylidene)-
    2. Synonyms:
    3. CAS NO:69982-05-4
    4. Molecular Formula: C21H17N2PS
    5. Molecular Weight: 360.419
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69982-05-4.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: 2-Thiazolamine, N-(triphenylphosphoranylidene)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Thiazolamine, N-(triphenylphosphoranylidene)-(69982-05-4)
    11. EPA Substance Registry System: 2-Thiazolamine, N-(triphenylphosphoranylidene)-(69982-05-4)

  • 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: 69982-05-4(Hazardous Substances Data)

69982-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69982-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,8 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69982-05:
(7*6)+(6*9)+(5*9)+(4*8)+(3*2)+(2*0)+(1*5)=184
184 % 10 = 4
So 69982-05-4 is a valid CAS Registry Number.

69982-05-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(1,3-thiazol-2-ylimino)-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names triphenyl(1,3-thiazol-2-ylimino)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69982-05-4 SDS

69982-05-4Relevant articles and documents

Three-component reaction of triphenylphosphine, dialkyl acetylenedicarboxylates, and heterocyclic rings and the related iminophosphoranes

Anary-Abbasinejad, Mohammad,Hassanabadi, Alireza,Khaksari, Zahra

, p. 204 - 212 (2011/10/31)

Crystalline phosphorus ylides are obtained in excellent yields from the 1:1:1 addition reaction of triphenylphosphine, dialkyl acetylenedicarboxylate, and NH acids, such as 2-aminothiazole and 2-aminobenzothiazole. These stabilized phosphoranes undergo a

Reaction between triphenylphosphine and aromatic amines in the presence of diethyl azodicarboxylate: An efficient synthesis of aryliminophosphoranes under neutral and mild conditions

Adib, Mehdi,Sheikhi, Ehsan,Deljoush, Azadeh

experimental part, p. 4137 - 4140 (2011/06/24)

An efficient synthesis of aryliminophosphoranes is described. A mixture of an aromatic amine, diethyl azodicarboxylate and triphenylphosphine undergo a Mitsonobu type reaction at ambient temperature in dry dichloromethane to afford aryliminophosphoranes in excellent yields.

Vinyltriphenylphosphonium salt-mediated efficient synthesis of iminophosphoranes derived from 2-aminothiazoles

Adib, Mehdi,Mostofi, Manizheh,Ghanbary, Khadijeh,Bijanzadeh, Hamid Reza

, p. 1663 - 1667 (2007/10/03)

Crystalline phosphorus ylides are obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine, dimethyl acetylenedicarboxylate and 2-aminothiazoles, such as 2-aminothiazole, 2-amino-3-methylthiazole, 2-aminothiazoline, 2-aminobenzothiazole, or 2-amino-7-methylbenzothiazole. These stabilized phosphoranes undergo a smooth intramolecular reaction in boiling toluene to produce the corresponding iminophosphoranes in excellent yields. Georg Thieme Verlag Stuttgart.

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