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1-(adamantane-2-yl)-3-benzylthiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29456-84-6 Structure
  • Basic information

    1. Product Name: 1-(adamantane-2-yl)-3-benzylthiourea
    2. Synonyms: 1-(adamantane-2-yl)-3-benzylthiourea
    3. CAS NO:29456-84-6
    4. Molecular Formula:
    5. Molecular Weight: 300.468
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29456-84-6.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: 1-(adamantane-2-yl)-3-benzylthiourea(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(adamantane-2-yl)-3-benzylthiourea(29456-84-6)
    11. EPA Substance Registry System: 1-(adamantane-2-yl)-3-benzylthiourea(29456-84-6)
  • 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: 29456-84-6(Hazardous Substances Data)

29456-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29456-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,5 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29456-84:
(7*2)+(6*9)+(5*4)+(4*5)+(3*6)+(2*8)+(1*4)=146
146 % 10 = 6
So 29456-84-6 is a valid CAS Registry Number.

29456-84-6Downstream Products

29456-84-6Relevant articles and documents

Gram Scalable Method to Synthesize Biscarbodiimides and Asymmetric Monocarbodiimides: A Platform to Access an Array of Phosphaguanidines, Amidines, and Guanidines

Bailey, Brad,Camelio, Andrew M.,Davis, Anna,Krasovskiy, Arkady

, (2021/11/12)

A mild, broadly functional group tolerant methodology has been developed to access a variety of mono- and bis-carbodiimides in good yield and high purity on multigram scale. Direct addition into these versatile motifs facilitated the rapid synthesis of a library of novel amidinines, guanidines, and phosphaguandines.

Pos [...] 4 group metal olefin polymerization catalyst

-

Paragraph 0469-0470, (2019/08/27)

Embodiments are directed to phosphaguanidine metal complexes of formula I and using those complexes in α-olefin polymerization systems.

Synthesis of adamantyl-containing 1,3-disubstituted diureas and thioureas, efficient targeted inhibitors of human soluble epoxide hydrolase

Butov,Burmistrov,Danilov,Pitushkin,Morisseau,Hammock

, p. 1569 - 1575 (2016/05/19)

A series of adamantyl-containing 1,3-disubstituted diureas and thioureas containing different spacers between the ureylene group and the adamantyl substituent has been synthesized, their inhibitory activity against mammalian and human soluble epoxide hydr

Highly efficient and catalyst-free synthesis of unsymmetrical thioureas under solvent-free conditions

Halimehjani, Azim Ziyaei,Pourshojaei, Yaghoub,Saidi, Mohammad R.

scheme or table, p. 32 - 34 (2009/04/10)

A highly efficient and simple synthesis of unsymmetrical thioureas is reported based on the reaction of readily synthesized dithiocarbamates with amines, without using any catalyst under solvent-free conditions. The short reaction time, high yields, and s

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