Welcome to LookChem.com Sign In|Join Free
  • or
5-methyl-8,9,10,11-tetrahydro[1]benzothieno[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine is a complex organic compound with a unique chemical structure. It belongs to the class of heterocyclic compounds, specifically a benzothienotriazolotriazolopyrimidine derivative. 5-methyl-8,9,10,11-tetrahydro[1]benzothieno[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine is characterized by the presence of a benzene ring fused with a thiophene ring, a triazole ring, and a pyrimidine ring. The molecule also features a methyl group attached to the pyrimidine ring. Due to its complex structure, this chemical may have potential applications in various fields, such as pharmaceuticals or materials science, although specific uses are not mentioned here. The compound's properties, reactivity, and potential applications would be determined by its molecular structure and the functional groups present.

77995-40-5

Post Buying Request

77995-40-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

77995-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77995-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,9 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77995-40:
(7*7)+(6*7)+(5*9)+(4*9)+(3*5)+(2*4)+(1*0)=195
195 % 10 = 5
So 77995-40-5 is a valid CAS Registry Number.

77995-40-5SDS

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 1,2,4-triazolo<2,3-c>-5-methyl-8,9,10,11-tetrahydrobenzo<b>thieno<3,2-e>pyrimidine

1.2 Other means of identification

Product number -
Other names 1,2,4-triazolo[2,3-c]-5-methyl-8,9,10,11-tetrahydrobenzo[b]thieno[3,2-e]pyrimidine

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:77995-40-5 SDS

77995-40-5Relevant academic research and scientific papers

Synthesis and pharmacological evaluation of novel thienopyrimidine and triazolothienopyrimidine derivatives

Mulla, Jameel Ahmed S.,Khazi, Mohammed Iqbal A.,Panchamukhi, Shridhar I.,Gong, Young-Dae,Khazi, Imtiyaz Ahmed M.

, p. 3235 - 3243 (2014/05/06)

Novel tricyclic thienopyrimidines (2, 3, 5, 8) and triazole-fused tetracyclic thienopyrimidines (6a-c and 9a-c) were synthesized from the precursor 2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile (1). The structures of newly synthesized compounds were established by spectral and analytical data. The title compounds were screened for analgesic, anti-inflammatory, ulcerogenicity index, and antibacterial activities. Test compounds exhibited significant activity, the compounds (6a-c) and (9a-c) showed more potent analgesic activity, and the compounds (6c) and (9c) showed more potent anti-inflammatory activity than the reference standard Diclofenac Sodium. All the synthesized compounds exhibited remarkable antibacterial activity.

Studies on the Synthesis and Interconversion of Isomeric Triazolothienopyrimidines. Part III. Cyclization Reactions of 2-Amino-3-(1H-1,2,4-triazol-3-yl)thiophenes

Shishoo, C. J.,Devani, M. B.,Ullas, G. V.,Ananthan, S.,Bhadti, V. S.

, p. 1125 - 1131 (2007/10/02)

Isolation of 2-amino-3-(1H-1,2,4-triazol-3-yl)thiophenes in the hydrolytic cleavage reactions of isomeric triazolothienopyrimidines is reported.The 2-amino-3-triazolylthiophenes on reaction with one carbon donors were found to cyclize to 1,2,4-triazolothienopyrimidines, exclusively.

Studies in the Synthesis and Interconversion of Isomeric Triazolothienopyrimidines

Shishoo, C. J.,Devani, M. B.,Ullas, G. V.,Anathan, S.,Bhadti, V. S.

, p. 43 - 46 (2007/10/02)

4-Hydrazinothienopyrimidines were cyclized with triethyl orthoformate and formic acid to give 1,2,4-triazolothienopyrimidines and 1,2,4-triazolothienopyrimidines depending on the reaction conditions employed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 77995-40-5
  • ©2008 LookChem.com,License:ICP NO.:Zhejiang16009103 complaints:service@lookchem.com
  • [Hangzhou]86-0571-87562588,87562578,87562573 Our Legal adviser: Lawyer