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CAS

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419532-33-5

6H-1,2,3,4,5,7-Pentathiazocine, dihydro-7-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 419532-33-5 Structure

  • Basic information

    1. Product Name: 6H-1,2,3,4,5,7-Pentathiazocine, dihydro-7-phenyl-
    2. Synonyms:
    3. CAS NO:419532-33-5
    4. Molecular Formula: C8H9NS5
    5. Molecular Weight: 279.496
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 419532-33-5.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: 6H-1,2,3,4,5,7-Pentathiazocine, dihydro-7-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6H-1,2,3,4,5,7-Pentathiazocine, dihydro-7-phenyl-(419532-33-5)
    11. EPA Substance Registry System: 6H-1,2,3,4,5,7-Pentathiazocine, dihydro-7-phenyl-(419532-33-5)

  • 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: 419532-33-5(Hazardous Substances Data)

419532-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 419532-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,9,5,3 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 419532-33:
(8*4)+(7*1)+(6*9)+(5*5)+(4*3)+(3*2)+(2*3)+(1*3)=145
145 % 10 = 5
So 419532-33-5 is a valid CAS Registry Number.

419532-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-phenyl-1,2,3,4,5,7-pentathiazocane

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:419532-33-5 SDS

419532-33-5Relevant articles and documents

Synthesis and oxidative ring contraction of 1,5,3,7-dichalcogenadiazocanes. Novel formation of 1,2,4-diselenazolidines, 1,2,4-ditellurazolidines, and 1,2,3,4,5,7-pentathiazocanes

Takikawa, Yuji,Koyama, Yutaka,Yoshida, Takamasa,Makino, Kenshiro,Shibuya, Hiroki,Sato, Kazuto,Otsuka, Tatsuya,Shibata, Yuko,Onuma, Yuki,Aoyagi, Shigenobu,Shimada, Kazuaki,Kabuto, Chizuko

, p. 1913 - 1925 (2007/10/03)

1,5,3,7-Dithiadiazocanes, 1,5,3,7-diselenadiazocanes, and 1,5,3,7-ditelluradiazocanes were prepared from a primary amine, formalin, and H2S, NaSeH, or NaTeH, respectively. Oxidation of 1,5,3,7- diselenadiazocanes and 1,5,3,7-ditelluradiazocanes using NBS efficiently afforded 1,2,4-diselenazolidines or 1,2,4-ditellurazolidines, respectively. In contrast, treatment of 1,5,3,7-dithiadiazocanes with bromine-elemental sulfur or disulfur dichloride (S2Cl2) afforded 1,2,3,4,5,7- pentathiazocanes. An unusual oxidative conversion of 1,5,3,7- dichalcogenadiazocanes into these products was assumed to proceed through in situ formation of 1,5,3,7-dichalcogenadiazabicyclo[3.3.0]octane-type dications.

Novel synthesis and thermal ring fission of 7-aryl-1,2,3,4,5,7-pentathiazocanes

Shimada, Kazuaki,Yoshida, Takamasa,Makino, Kenshiro,Otsuka, Tatsuya,Onuma, Yuki,Aoyagi, Shigenobu,Takikawa, Yuji,Kabuto, Chizuko

, p. 90 - 91 (2007/10/03)

Treatment of 1,5,3,7-dithiadiazocanes 1 with bromine-elemental sulfur or disulfur dichloride (S2Cl2) afforded 1,2,3,4,5,7-pentathiazocanes 3, and heating of 3 caused unusual thermal ring fission to give an inseparable mixture of polysulfide chains bearing a thioformamide moiety on each terminal.

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