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CAS

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15438-85-4

1,3,5-Triazine-2,4-diamine,N2,N2,N4,N4-tetraethyl-6-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 15438-85-4 Structure

  • Basic information

    1. Product Name: 1,3,5-Triazine-2,4-diamine,N2,N2,N4,N4-tetraethyl-6-methoxy-
    2. Synonyms: 1,3,5-Triazine-2,4-diamine,N,N,N',N'-tetraethyl-6-methoxy- (9CI); s-Triazine, 2,4-bis(diethylamino)-6-methoxy-(7CI,8CI); Tetraetatone
    3. CAS NO:15438-85-4
    4. Molecular Formula: C12H23 N5 O
    5. Molecular Weight: 253.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15438-85-4.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: 1,3,5-Triazine-2,4-diamine,N2,N2,N4,N4-tetraethyl-6-methoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3,5-Triazine-2,4-diamine,N2,N2,N4,N4-tetraethyl-6-methoxy-(15438-85-4)
    11. EPA Substance Registry System: 1,3,5-Triazine-2,4-diamine,N2,N2,N4,N4-tetraethyl-6-methoxy-(15438-85-4)

  • 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: 15438-85-4(Hazardous Substances Data)

15438-85-4 Usage

Chemical classification

Derivative of 1,3,5-triazine (a heterocyclic aromatic compound)

Applications

Production of dyes and pigments
Synthesis of pharmaceuticals and agrochemicals
Intermediate in the production of other chemicals

Chemical properties

Strong electron-donating properties

Usage

Commonly used in organic synthesis reactions

Check Digit Verification of cas no

The CAS Registry Mumber 15438-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,3 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15438-85:
(7*1)+(6*5)+(5*4)+(4*3)+(3*8)+(2*8)+(1*5)=114
114 % 10 = 4
So 15438-85-4 is a valid CAS Registry Number.

15438-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N,2-N,4-N,4-N-tetraethyl-6-methoxy-1,3,5-triazine-2,4-diamine

1.2 Other means of identification

Product number -
Other names 1,3,5-Triazine-2,4-diamine,N,N,N',N'-tetraethyl-6-methoxy

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:15438-85-4 SDS

15438-85-4Downstream Products

15438-85-4Relevant articles and documents

Synthesis and antiviral evaluation of some C3-symmetrical trialkoxy-substituted 1,3,5-triazines and their molecular geometry

Mibu, Nobuko,Yokomizo, Kazumi,Aki, Hatsumi,Ota, Norimasa,Fujii, Hiroyuki,Yuzuriha, Ai,Saneyoshi, Shiori,Tanaka, Aoi,Koga, Airi,Zhou, Jianrong,Miyata, Takeshi,Sumoto, Kunihiro

, p. 935 - 944 (2015)

As one of our projects, we here report some new molecular modifications of 2,4,6-trichloro-1,3,5-triazine (TCTAZ: 1) to symmetrical 2,4,6-trialkoxy- or 2,4,6-triaryloxy-substituted 1,3,5-triazine (TAZ) molecules, as well as the results of anti-herpes simplex virus type 1 (anti-HSV-1) activity evaluation of synthesized 2,4,6-trisubstituted TAZ derivatives. Among the tested 2,4,6-trisubstituted TAZ derivatives, we reconfirmed that a C3-symmetrical TAZ derivative, 4e, shows the highest level of anti-HSV-1 activity with a good selectivity index. In this paper, we also report the results of the preparation of newly targeted TAZ derivatives and the structure-activity relationships (SARs) of these trialkoxy-substituted TAZ derivatives and related compounds. The sugar recognition properties of C3-symmetrical TAZ derivative 4e are also described.

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