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2-methyl-4H-[1,3]thiazino[3,2-a]benzimidazol-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64411-76-3

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64411-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64411-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,1 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64411-76:
(7*6)+(6*4)+(5*4)+(4*1)+(3*1)+(2*7)+(1*6)=113
113 % 10 = 3
So 64411-76-3 is a valid CAS Registry Number.

64411-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-[1,3]thiazino[3,2-a]benzimidazol-4-one

1.2 Other means of identification

Product number -
Other names 2-methyl-benzo[4,5]imidazo[2,1-b][1,3]thiazin-4-one

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:64411-76-3 SDS

64411-76-3Downstream Products

64411-76-3Relevant academic research and scientific papers

Palladium-Catalyzed Cyclocarbonylation Approach to Thiadiazafluorenones: A Correction

Veltri, Lucia,Amuso, Roberta,Cuocci, Corrado,Vitale, Paola,Gabriele, Bartolo

, p. 8743 - 8749 (2019)

The palladium-catalyzed carbonylation of 2-(propynylthio)benzimidazoles bearing a terminal triple bond leads to 2-methyl-1-thia-4a,9-diazafluoren-4-ones instead of the previously reported 3-methyl isomers, as unequivocally established by XRD analysis of a representative product. A correction is therefore provided here in order to rectify the previous erroneous assignment of the position of the methyl group. Moreover, the process has been generalized to substrates bearing an internal triple bond, which lead to 3-alkyl-2-methyl-1-thia-4a,9-diazafluoren-4-ones, whose structure was confirmed by XRD analysis of two representative derivatives.

N-Heterocyclic Carbene-Catalyzed in situ Activation of Alkynyl Acids for C?S Bond Formation: Access to Imidazo[2,1-b][1,3]thiazinones

Sun, Kewen,Jin, Shiyi,Zhu, Jindong,Zhang, Xinmiao,Gao, Maoyu,Zhang, Wanqi,Lu, Tao,Du, Ding

, p. 4515 - 4522 (2018/10/24)

Alkynyl acids are first utilized as alkynyl acylazolium precursors through an in situ activation strategy for the efficient construction of carbon-sulfur bond in a formal [3+3] annulation. This protocol offers a direct and rapid pathway for the synthesis of imidazo[2,1-b][1,3]thiazinone skeleton, a useful heterocyclic class frequently found in many bioactive compounds. This reaction also has the advantages of scalability, readily available materials, and simple manipulation in open air. (Figure presented.).

Addition Reactions of Diketene. IV. Reaction of Diketene with Thioureas, Thioamide, and Aminothiol

Sakamoto, Masanori,Akimoto, Takashi,Fukutomi, Kyoko,Ishii, Keitaro

, p. 2516 - 2521 (2007/10/02)

The reaction of benzimidazoline-2-thione (2) with diketene (1) gave the oxazine derivative 3 and the thiazine derivative 4.However, the reaction of 2-indolinethione (6) with diketene afforded only the thiazine derivative 7.On the other hand, no cyclized compound was obtained from 2-indolinone (8) and diketene.The reactions of N,N'-diphenylthiourea (11) and 2-aminobenzothiol (14) with diketene were also studied; 11 and 14 gave the thiouracil 12 and the benzothiazine 16, respectively.Keywords: diketene; thiourea; thioamide; aminothiol; cyclization; 1,3-oxazine; 1,3-thiazine; thiouracil; thiazepine.

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