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CAS

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2608-11-9

HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE is a chemical compound with potent antimicrobial properties, commonly utilized as a fungicide and bactericide in agricultural applications. It is effective against a broad spectrum of plant pathogens and contributes to disease control and crop protection by inhibiting the growth and reproduction of fungi and bacteria. Its low toxicity to humans and animals makes it a safe and reliable choice for agricultural use.

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  • Hexahydro-1H-azepine-1-carbodithioic acid, compd. with hexahydro-1H-azepine (1:1)

    Cas No: 2608-11-9

  • USD $ 1.9-2.9 / Gram

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  • 2608-11-9 Structure

  • Basic information

    1. Product Name: HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE
    2. Synonyms: HEXAMETHYLENEDITHIOCARBAMIC ACID HEXAMETHYLENEAMMONIUM SALT;HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE;hexahydro-1h-azepine-1-carbodithioicacicompd.withhexahydro-1h-azepine(;hexahydro-1H-azepine-1-dithiocarboxylic acid, compound with hexahydro-1H-azepine (1:1);Hexamethylenedithiocarbamicacidhexamethyleneimin;N,N-Hexamethylenedithiocarbamicacidhexamethyleneiminiumsalt=HexamethyleneammoniumHexamethylenedithiocarbamate;1H-Azepine-1-carbodithioic acid, hexahydro-, compd. with hexahydro-1H-azepine (1:1);Hexahydro-1H-azepine·hexahydro-1H-azepine-1-dithiocarboxylic acid
    3. CAS NO:2608-11-9
    4. Molecular Formula: C6H13N*C7H13NS2
    5. Molecular Weight: 274.49
    6. EINECS: 220-023-1
    7. Product Categories: N/A
    8. Mol File: 2608-11-9.mol

  • Chemical Properties

    1. Melting Point: 146.0 to 149.0 °C
    2. Boiling Point: 242.7°Cat760mmHg
    3. Flash Point: 100.6°C
    4. Appearance: /
    5. Density: g/cm3
    6. Vapor Pressure: 0.0335mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE(2608-11-9)
    12. EPA Substance Registry System: HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE(2608-11-9)

  • 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: 2608-11-9(Hazardous Substances Data)

2608-11-9 Usage

Uses

Used in Agricultural Applications:
HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE is used as a fungicide and bactericide for its strong antimicrobial properties, which help in controlling a wide range of plant pathogens and protecting crops from diseases.
Used in Pest and Disease Management:
HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE is used as a component in integrated pest and disease management strategies, often in combination with other chemicals, to provide a comprehensive approach to maintaining crop health and productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 2608-11-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,0 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2608-11:
(6*2)+(5*6)+(4*0)+(3*8)+(2*1)+(1*1)=69
69 % 10 = 9
So 2608-11-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NS2.C6H13N/c9-7(10)8-5-3-1-2-4-6-8;1-2-4-6-7-5-3-1/h1-6H2,(H,9,10);7H,1-6H2

2608-11-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name azepane,azepane-1-carbodithioic acid

1.2 Other means of identification

Product number -
Other names Hexahydro-1H-azepine-1-carbodithioic acid,compd. with hexahydro-1H-azepine (1:1)

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:2608-11-9 SDS

2608-11-9Downstream Products

2608-11-9Relevant articles and documents

Cu-mediated one-pot three-component synthesis of 3-N-substituted 1,4,2-benzodithiazine 1,1-dioxide derivatives

Dong, Wei,Ge, Zemei,Wang, Xin,Li, Ridong,Li, Runtao

, (2020/07/03)

A novel and efficient copper-catalyzed one-pot procedure for the synthesis of 3-N-substituted 1,4,2-benzodithiazine 1,1-dioxide derivatives from 2-halobenzenesulfonamides, amines and CS2 is described. The reaction proceeds through Ullmann-type S-arylation, intramolecular addition of NH2 with C[dbnd]S and dehydrosulfide, which provides a new and useful strategy for construction of cyclic aromatic sulfonamides.

A catalyst-free 1,4-Michael-type reaction of in situ generated ortho-quinone methides (o-QMs) with dithiocarbamic acid salts in water

Aryanasab, Fezzeh,Shabanian, Meisam

, p. 1703 - 1713 (2019/04/17)

Abstract: A catalyst-free conjugate addition of dithiocarbamic acid salts to in situ generated ortho-quinone methides (o-QMs) was investigated for the first time. Several dithiocarbamate derivatives of 4-hydroxycoumarine, 4-hydroxypyrone and 2-naphthol were synthesized in moderate-to-good yields in water at room temperature. Graphical abstract: [Figure not available: see fulltext.] Catalyst-free addition of dithiocarbamic acid salts to in situ generated o-QMs in water at room temperature.

Investigation of the reaction of dithiocarbamic acid salts with trimethyl orthoformate and styrene epoxide

Ziyaei Halimehjani, Azim,Hajilou Shayegan, Mojtaba,Poshteh, Shiva Shakori,Amani, Vahid,Notash, Behrouz,Hashemi, Mohammad M.

supporting information, p. 7124 - 7127 (2015/12/05)

The reaction of dithiocarbamic acid salts with trimethyl orthoformate in the presence of BF3·OEt2 was investigated to give 4-(N,N-dialkyldithiocarbamato)-2-dialkyliminio-1,3-dithietane tetrafluoroborates in good yields. Additionally, a one-pot procedure for the synthesis of 2-iminium-1,3-dithiolanes from the BF3·OEt2 catalyzed reaction of dithiocarbamic acid salts with styrene epoxide is described.

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