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113274-26-3

2-Triazene-1-carboxylic acid, 3-(2-hydroxyethyl)-1-methyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2-Triazene-1-carboxylic acid,3-(2-hydroxyethyl)-1-methyl-,ethyl ester

    Cas No: 113274-26-3

  • USD $ 1.9-2.9 / Gram

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  • 113274-26-3 Structure

  • Basic information

    1. Product Name: 2-Triazene-1-carboxylic acid, 3-(2-hydroxyethyl)-1-methyl-, ethyl ester
    2. Synonyms: 2-Triazene-1-carboxylic acid, 3-(2-hydroxyethyl)-1-methyl-, ethyl ester
    3. CAS NO:113274-26-3
    4. Molecular Formula: C6H13N3O3
    5. Molecular Weight: 175.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113274-26-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Triazene-1-carboxylic acid, 3-(2-hydroxyethyl)-1-methyl-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Triazene-1-carboxylic acid, 3-(2-hydroxyethyl)-1-methyl-, ethyl ester(113274-26-3)
    11. EPA Substance Registry System: 2-Triazene-1-carboxylic acid, 3-(2-hydroxyethyl)-1-methyl-, ethyl ester(113274-26-3)

  • 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: 113274-26-3(Hazardous Substances Data)

113274-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113274-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113274-26:
(8*1)+(7*1)+(6*3)+(5*2)+(4*7)+(3*4)+(2*2)+(1*6)=93
93 % 10 = 3
So 113274-26-3 is a valid CAS Registry Number.

113274-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-carbethoxy--2-(hydroxyethyl)-3-methyltriazene

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:113274-26-3 SDS

113274-26-3Relevant articles and documents

Novel Cross-Linking Alkylating Agents, 1-(2-Chloroethyl)-3-methyl-3-acyltriazenes

Smith, Richard H.,Mehl, Andrew F.,Shantz, Donald L.,Chmurny, Gwendolyn N.,Michejda, Christopher J.

, p. 1467 - 1471 (1988)

The preparation and hydrolytic decomposition of a series of novel cross-linking alkylating agents, 1-(2-chloroethyl)-3-methyl-3-acyltriazenes, is described.The synthesis 3-carbethoxy-1-(2-chloroethyl)-3-methyltriazene, 3-acetyl-1-(2-chloroethyl)-3-methyltriazene, and 1-(2-chloroethyl)-3-methyl-3-(methylcarbamoyl)triazene has been accomplished through the use of a common intermediate, 1--3-methyltriazene, bearing a key protecting group on the 2-ethyl position.Following acylation, the blocking group was removed with tetra-n-butylammoniu m fluoride and the resulting alcohol was converted to the desired chloro substituent by reaction with carbon tetrachloride and triphenylphosphine.Kinetic studies on the proteolytic decomposition at neutral pH of the (2-chloroethyl)triazenes, the corresponding (2-hydroxyethyl)triazenes, and the analogous 1,3-dimethyl-3-acyltriazenes revealed that the reactions proceed by N2-N3 heterolysis.The rates of the reactions are dependent on the stabilities of the incipient alkyldiazonium ions and on the ability of the 3-acyl substituens to stabilize the adjacent nagative charge.

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