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Phenol, 4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2,6-bis(1,1-dimethylethyl)-, also known as a triazine-based herbicide, is a chemical compound characterized by its phenol group and two tert-butyl groups. The incorporation of the 4,6-dichloro-1,3,5-triazin-2-yl group significantly amplifies its herbicidal efficacy by inhibiting specific plant enzymes. Phenol,
4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2,6-bis(1,1-dimethylethyl)is recognized for its high toxicity, necessitating careful handling and stringent regulatory measures in various countries to mitigate its environmental and health risks.

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  • 976-09-0 Structure
  • Basic information

    1. Product Name: Phenol, 4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2,6-bis(1,1-dimethylethyl)-
    2. Synonyms:
    3. CAS NO:976-09-0
    4. Molecular Formula: C17H22Cl2N4O
    5. Molecular Weight: 369.294
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 976-09-0.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: Phenol, 4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2,6-bis(1,1-dimethylethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2,6-bis(1,1-dimethylethyl)-(976-09-0)
    11. EPA Substance Registry System: Phenol, 4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2,6-bis(1,1-dimethylethyl)-(976-09-0)
  • 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: 976-09-0(Hazardous Substances Data)

976-09-0 Usage

Uses

Used in Agricultural Industry:
Phenol, 4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2,6-bis(1,1-dimethylethyl)is utilized as a potent herbicide for controlling a broad spectrum of weeds in various crops. Its application is aimed at enhancing crop yield by minimizing competition from unwanted plant species, thus ensuring the healthy growth of cultivated plants.
Used in Pest Control:
In the pest control sector, this chemical compound serves as an effective pesticide, targeting and eliminating a range of pests that can damage crops and gardens. Its use in this context is driven by its ability to disrupt essential biological processes in pests, thereby protecting plants from infestation and potential yield loss.

Check Digit Verification of cas no

The CAS Registry Mumber 976-09-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,7 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 976-09:
(5*9)+(4*7)+(3*6)+(2*0)+(1*9)=100
100 % 10 = 0
So 976-09-0 is a valid CAS Registry Number.

976-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-di-tert-butyl-4-(4,6-dichloro-[1,3,5]triazin-2-ylamino)-phenol

1.2 Other means of identification

Product number -
Other names 2,6-Di-tert-butyl-4-(4,6-dichloro-[1,3,5]triazin-2-ylamino)-phenol

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:976-09-0 SDS

976-09-0Relevant articles and documents

SUBSTITUTED TRIAZINE COMPOUNDS AND USES THEREOF

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Page/Page column 25-26; 36, (2021/07/17)

The present invention relates to compounds of formula (I) : including any stereochemically isomeric form thereof, or pharmaceutically acceptable salts thereof, for the treatment of, for example, hypercholesterolemia.

Phenolic amine compound and preparation method and application thereof

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Paragraph 0099; 0104-0105; 0119-0120; 0124-0125; 0139-0140, (2020/07/21)

The invention relates to a phenolic amine compound as well as a preparation method and an application thereof. The phenolic amine compound has a structure as shown in a formula V, and not only has excellent oxidation resistance, but also has very good lubricating property.

SYNTHESIS AND PROPERTIES OF sym-TRIAZINE DERIVATIVES. 2. SYNTHESIS OF AMINO-sym-TRIAZINES CONTAINING FRAGMENTS OF STERICALLY HINDERED PHENOL

Malova, O. V.,Vishnyakova, T. P.,Golubeva, I. A.,Kelarev, V. I.,Lunin, A. F.

, p. 1384 - 1388 (2007/10/02)

The reaction of mono- and dichloro-sym-triazines with 4-hydroxy-3,5-di-tert-butylaniline was studied.N-substituted derivatives of 2,4,6-triamino-sym-triazine were synthesized, containing fragments of sterically hindered phenol.

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