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ETHYL 2-[(METHYLAMINO)CARBONYL]HYDRAZINECARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13482-66-1

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13482-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13482-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,8 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13482-66:
(7*1)+(6*3)+(5*4)+(4*8)+(3*2)+(2*6)+(1*6)=101
101 % 10 = 1
So 13482-66-1 is a valid CAS Registry Number.

13482-66-1SDS

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 ethyl N-(methylcarbamoylamino)carbamate

1.2 Other means of identification

Product number -
Other names 1-Ethoxycarbonyl-4-methyl-semicarbazid

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:13482-66-1 SDS

13482-66-1Relevant academic research and scientific papers

Preparation of 2-(alkylcarbamoyl)hydrazine-1-carboxylic acid alkyl ester or its corresponding urazole salt

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Paragraph 0128-0130, (2021/06/23)

The present invention relates to the preparation of 2-(alkylcarbamoyl)hydrazine-1-carboxylic acid alkyl ester or its corresponding urazole salt. The present invention relates to 2-(alkylcarbamoyl)hydrazine-1-alkyl carboxylate or its corresponding derivative alkyl-4H-1,2,4-triazole-3,5-diol salt (urine Azole salt) preparation. This is particularly advantageous because it uses a one-pot reaction and uses alkyl acetate as the solvent in steps a) and b) of its synthesis.

Development of a Scalable and Sublimation-Free Route to MTAD

Siddiqi, Zohaib R.,Ungarean, Chad N.,Bingham, Tanner W.,Sarlah, David

, p. 2953 - 2959 (2020/12/21)

The cyclic azodicarbonyl 4-methyl-1,2,4-triazoline-3,5-dione (MTAD) is a versatile and powerful reagent used mainly in cycloaddition chemistry. Though known for more than 50 years, its unsafe preparation, as well as purification by sublimation, hampered i

METHOD FOR PRODUCING SEMICARBAZIDE COMPOUND, AND METHOD FOR PRODUCING TRIAZOLIDINEDIONE COMPOUND

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Paragraph 0129; 0132-0136, (2020/02/14)

PROBLEM TO BE SOLVED: To provide a method for synthesizing a semicarbazide compound which gives the semicarbazide compound without passing through an acyl azide. SOLUTION: Carbonylating agents such as carbonyl diimidazole (CDI) and triphosgene (TCF) are brought into contact with either one of an amine compound and a carbazate compound to form an active intermediate. A semicarbazide compound is synthesized by reacting the resulting active intermediate with the remaining one of the amine compound and the carbazate compound. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Alternative synthetic routes to N-methyl-1,2,4-triazoline-3,5-dione (MeTAD) and other triazolinedione derivatives

Breton, Gary W.,Turlington, Mark

supporting information, p. 4661 - 4663 (2015/02/19)

N-Methyl-1,2,4-triazoline-3,5-dione (MeTAD) is a powerful electrophile and a versatile synthetic reagent. In this Letter we describe two methods for the synthesis of N-methylurazole, the direct precursor to MeTAD, on gram scales and in good yields. Both methods provide pure urazole while avoiding the necessity of large scale purification via column chromatography or recrystallization. One of the methods proved to be amenable for the synthesis of derivatives other than N-methyl.

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