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10-bromoanthracen-9-yl dipropan-2-ylcarbamodithioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1-(10-bromoanthracen-9-yl)sulfanyl-N,N-dipropan-2-yl-methanethioamide

    Cas No: 82884-33-1

  • USD $ 1.9-2.9 / Gram

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  • 82884-33-1 Structure
  • Basic information

    1. Product Name: 10-bromoanthracen-9-yl dipropan-2-ylcarbamodithioate
    2. Synonyms:
    3. CAS NO:82884-33-1
    4. Molecular Formula: C21H22BrNS2
    5. Molecular Weight: 432.4401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82884-33-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 540.8°C at 760 mmHg
    3. Flash Point: 280.9°C
    4. Appearance: N/A
    5. Density: 1.38g/cm3
    6. Vapor Pressure: 9.25E-12mmHg at 25°C
    7. Refractive Index: 1.704
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 10-bromoanthracen-9-yl dipropan-2-ylcarbamodithioate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 10-bromoanthracen-9-yl dipropan-2-ylcarbamodithioate(82884-33-1)
    12. EPA Substance Registry System: 10-bromoanthracen-9-yl dipropan-2-ylcarbamodithioate(82884-33-1)
  • 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: 82884-33-1(Hazardous Substances Data)

82884-33-1 Usage

Molecular structure

A complex chemical compound consisting of a 10-bromoanthracen-9-yl group and a dipropan-2-ylcarbamodithioate group.

10-bromoanthracen-9-yl group

A derivative of anthracene, a polycyclic aromatic hydrocarbon, with a bromine atom attached at the 10th position.

Dipropan-2-ylcarbamodithioate group

A carbamate derivative with two propyl groups attached to the nitrogen atom.

Chemical classification

A carbamate derivative, which is a type of organic compound containing a carbonyl group (C=O) bonded to a nitrogen atom.

Potential applications

Fields such as organic synthesis, materials science, and pharmaceuticals may benefit from the unique properties of this compound.

Unique structure

The combination of the 10-bromoanthracen-9-yl group and the dipropan-2-ylcarbamodithioate group results in a distinctive molecular structure.

Further study

The compound's properties and potential applications make it an interesting subject for research and development.

Chemical properties

The compound may exhibit various chemical properties, such as reactivity, solubility, and stability, which can be explored through experimental studies.

Synthesis

The compound can be synthesized through chemical reactions involving the 10-bromoanthracen-9-yl group and the dipropan-2-ylcarbamodithioate group.

Safety and handling

As with any chemical compound, proper safety precautions and handling procedures should be followed to minimize risks during experimentation and application.

Check Digit Verification of cas no

The CAS Registry Mumber 82884-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,8 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82884-33:
(7*8)+(6*2)+(5*8)+(4*8)+(3*4)+(2*3)+(1*3)=161
161 % 10 = 1
So 82884-33-1 is a valid CAS Registry Number.

82884-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (10-bromoanthracen-9-yl) N,N-di(propan-2-yl)carbamodithioate

1.2 Other means of identification

Product number -
Other names -

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:82884-33-1 SDS

82884-33-1Downstream Products

82884-33-1Relevant articles and documents

A NEW SYNTHESIS OF AROMATIC THIOLS

Jen, Kwan-Yue,Cava, Michael P.

, p. 2001 - 2004 (2007/10/02)

Benzenoid and heterocyclic lithio derivatives react smoothly with tetraisopropylthiuram disulfide to give highly crystalline and readily purified S-aryl-N,N-diisopropyldithiocarbamates, which yield aromatic thiols on alkaline hydrolysis.

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