113748-39-3

• 

• Basic information

  1. Product Name: 4H-Thiopyrano[3,4-d]isoxazol-3(2H)-one,6,7-dihydro-(9CI)
  2. Synonyms: 4H-Thiopyrano[3,4-d]isoxazol-3(2H)-one,6,7-dihydro-(9CI)
  3. CAS NO:113748-39-3
  4. Molecular Formula: C6H7NO2S
  5. Molecular Weight: 157.19028
  6. EINECS: N/A
  7. Product Categories: OXAZOLE
  8. Mol File: 113748-39-3.mol
  9. Article Data: 1

• 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: 4H-Thiopyrano[3,4-d]isoxazol-3(2H)-one,6,7-dihydro-(9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 4H-Thiopyrano[3,4-d]isoxazol-3(2H)-one,6,7-dihydro-(9CI)(113748-39-3)
  11. EPA Substance Registry System: 4H-Thiopyrano[3,4-d]isoxazol-3(2H)-one,6,7-dihydro-(9CI)(113748-39-3)

• 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: 113748-39-3(Hazardous Substances Data)

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• 4H-Thiopyrano[3,4-d]isoxazol-3(2H)-one,6,7-dihydro-

  Cas No: 113748-39-3

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• Henan Tianfu Chemical Co., Ltd.
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113748-39-3 Usage

Classification

Organic heterocyclic compound

Structure

Bicyclic compound containing a thiopyran ring fused to an isoxazolone ring

Properties

Pharmaceutical and Biological Potential:
Potential for drug development and therapeutic agents
Pharmacological Activities:
Subject of interest in chemical and pharmaceutical research
Potential to exhibit various pharmacological activities
Applications:
Medicinal and industrial uses
Structural and Functional Properties:
Unique structural and functional properties

Significance

Subject of interest in chemical and pharmaceutical research
Important target for synthesis of novel drug molecules

Check Digit Verification of cas no

The CAS Registry Mumber 113748-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113748-39:
(8*1)+(7*1)+(6*3)+(5*7)+(4*4)+(3*8)+(2*3)+(1*9)=123
123 % 10 = 3
So 113748-39-3 is a valid CAS Registry Number.

113748-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	6,7-dihydro-4H-thiopyrano<3,4-d>isoxazol-3-ol

1.2 Other means of identification

Product number	-
Other names	6,7-Dihydro-4H-thiopyrano[3,4-d]isoxazol-3-ol

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:113748-39-3 SDS

113748-39-3Upstream product

• 113748-37-1 3-(ethoxycarbonyl)-2,3,5,6-tetrahydro-4-oxo-4H-thiopyran ethylene ketal 
• 1198-44-3 ethyl 4-oxotetrahydro-2H-thiopyran-3-carboxylate 
• 113748-38-2 2,3,5,6-tetrahydro-4-oxo-4H-thiopyran-3-carbohydrxamic acid ethylene ketal 

113748-39-3Downstream Products

113748-39-3Relevant articles and documents

Heterocyclic Muscarinic Agonists. Synthesis and Biological Activity of Some Bicyclic Sulfonium Arecoline Bioisosteres

Sauerberg, Per,Falch, Erik,Meier, Eddi,Lemboel, Hanne L.,Krogsgaard-Larsen, Povl

, p. 1312 - 1316 (2007/10/02)

A number of S-methylsulfonium analogues of the conformationally restricted muscarinic agonists of the 3-alkoxy-4,5,6,7-tetrahydroisoxazolopyridine (O-alkyl-THPO) type have been synthesized.The effects on muscarinic receptors of these 3-alkoxy-5-methyl-6,7-dihydro-4H-thiopyranoisoxazol-5-ium (O-alkyl-S-methyl-DHTO) analogues (7a-d) were assessed in receptor-binding experiments with tritiated oxotremorine M, pirenzepine, and quinuclidinyl benzilate as ligands and were supported by studies on the isolated quinea pig ileum.The degree of muscarinic agonist activity of the compounds (M-agonist index) and their selectivity for M-1 or M-2 muscarinic receptor subtypes (M-2/M-1 index) were estimated on the basis of receptor-binding studies.The in vitro pharmacological profiles of the compounds were compared with those of arecoline and its sulfonium and 3-methoxyisoxazole isosteres, sulfoarecoline and O,5-dimethyl-THPO, respectively.While O-methyl-DHTO (5a) and N-methyl-DHTO (6a) were inactive, all of the sulfonium analogues 7a-d were muscarinic agonists with the exception of O-ethyl-S-methyl-DHTO (7b), which showed a muscarinic antagonist profile.

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