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5H-1,2,4-Triazolo[3,4-b][1,3]thiazine, 6,7-dihydro-3,7-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94835-57-1

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94835-57-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94835-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,3 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94835-57:
(7*9)+(6*4)+(5*8)+(4*3)+(3*5)+(2*5)+(1*7)=171
171 % 10 = 1
So 94835-57-1 is a valid CAS Registry Number.

94835-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7-diphenyl-6,7-dihydro-5H-[1,2,4]triazolo[3,4-b][1,3]thiazine

1.2 Other means of identification

Product number -
Other names 5H-1,2,4-Triazolo[3,4-b][1,3]thiazine,6,7-dihydro-3,7-diphenyl

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:94835-57-1 SDS

94835-57-1Downstream Products

94835-57-1Relevant academic research and scientific papers

CYCLIZATION OF N1-(CINNAMYL-THIOCARBAMOYL)-AMIDRAZONES. PART I

Strzemecka, Leokadia

, p. 157 - 166 (2007/10/02)

The cyclization of N1-(cinnamyl-thiocarbamoyl)-amidrazones 1-3 with diluted and concentrated hydrochloric acid has been studied.Heterocyclic systems od 1,2,4-triazole A, 1,3,4-thiadiazole B, 1,2,4-triazole1,3-thiazine C and 1,3,4-thiadiazolepyrimidine D were obtained in good yields.Compounds 1-3 with diluted hydrochloric acid afforded systems A and B.Compound 1 yielded both heterocyclic systems 1A and 1B, whereas compounds 2, 3 yielded 2B, 3B only.The cyclization reaction of 1-3 with concentrated hydrochloric acid afforded the corresponding heterocyclic systems: 1C; 2C, 2D; 3B, 3C, 3D.The structure of the obtained compounds were proved by means of 1H NMR spectra.

CYCLIZATION REACTION OF 1,4-DISUBSTITUTED THIOSEMICARBAZIDES. PART I

Strzemecka, Leokadia,Otto, Teresa

, p. 757 - 766 (2007/10/02)

The cyclization reaction of 1-acyl(aroyl)-4-cinnamyl-thiosemicarbazides 1-7 with hydrochloric acid was carried out.Four various heterocyclic systems were obtained.Compounds 2-5 under cyclization form the 1,2,4-triazolo-1,3-thiazine system 2-5B.Comp

SYNTHESIS OF 5H-3,7-DISUBSTITUTED 6,7-DIHYDRO-1,2,4-TRIAZOLE1,3-THIAZINE AND 7H-2,5-DISUBSTITUTED 5,6-DIHYDRO-1,2,4-TRIAZOLE1,3-THIAZINE SYSTEMS

Strzemecka, Leokadia

, p. 881 - 886 (2007/10/02)

The cyclization reaction of 3-substituted 4-cinnamyl-1,2,4-triazole-5-thiones was investigated.Formation of isomeric 1,2,4-triazole1,3-thiazine and 1,2,4-triazole1,3-thiazine systems has been observed.The structure of the compounds obtained

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