121497-12-9

• 

• Basic information

  1. Product Name: dimethyl 4-{2-chloro-6-[4-(methoxycarbonyl)-2,5-dimethylfuran-3-yl]quinolin-3-yl}-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
  2. Synonyms:
  3. CAS NO:121497-12-9
  4. Molecular Formula: C₂₈H₂₇ClN₂O₇
  5. Molecular Weight: 538.9762
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 121497-12-9.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 640.6°C at 760 mmHg
  3. Flash Point: 341.2°C
  4. Appearance: N/A
  5. Density: 1.288g/cm³
  6. Vapor Pressure: 2.64E-16mmHg at 25°C
  7. Refractive Index: 1.586
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: dimethyl 4-{2-chloro-6-[4-(methoxycarbonyl)-2,5-dimethylfuran-3-yl]quinolin-3-yl}-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate(CAS DataBase Reference)
  11. NIST Chemistry Reference: dimethyl 4-{2-chloro-6-[4-(methoxycarbonyl)-2,5-dimethylfuran-3-yl]quinolin-3-yl}-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate(121497-12-9)
  12. EPA Substance Registry System: dimethyl 4-{2-chloro-6-[4-(methoxycarbonyl)-2,5-dimethylfuran-3-yl]quinolin-3-yl}-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate(121497-12-9)

• 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: 121497-12-9(Hazardous Substances Data)

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• SDS
• Upstream product
• Downstream Products
• Article

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• 3,5-Pyridinedicarboxylicacid,4-[2-chloro-6-[4-(methoxycarbonyl)-2,5-dimethyl-3-furanyl]-3-quinolinyl]-1,4-dihydro-2,6-dimethyl-,3,5-dimethyl ester

  Cas No: 121497-12-9

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121497-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121497-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,4,9 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121497-12:
(8*1)+(7*2)+(6*1)+(5*4)+(4*9)+(3*7)+(2*1)+(1*2)=109
109 % 10 = 9
So 121497-12-9 is a valid CAS Registry Number.

121497-12-9SDS

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	dimethyl 4-[2-chloro-6-(4-methoxycarbonyl-2,5-dimethylfuran-3-yl)quinolin-3-yl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

1.2 Other means of identification

Product number	-
Other names	3,5-Pyridinedicarboxylic acid,4-(2-chloro-6-(4-(methoxycarbonyl)-2,5-dimethyl-3-furanyl)-3-quinolinyl)-1,4-dihydro-2,6-dimethyl-,dimethyl ester

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:121497-12-9 SDS

121497-12-9Upstream product

• 89447-05-2 4-(4-acetamidophenyl)-2,5-dimethyl-3-(methoxycarbonyl)furan 
• 121497-04-9 2-chloro-6-<2,5-dimethyl-3-(methoxycarbonyl)furan-4-yl>-3-formylquinoline 
• 14205-39-1 methyl 3-aminocrotonate 

121497-12-9Downstream Products

121497-12-9Relevant articles and documents

Syntheses and bioevaluation of substituted dihydropyridines for pregnancy-interceptive activity in hamsters

Mukherjee,Akhtar,Sharma,Seth,Bhaduri,Agnihotri,Mehrotra,Kamboj

, p. 2297 - 2300 (2007/10/02)

A number of 2,6-dimethyl-3,5-bis(methoxycarbonyl)-4-substituted-1,4-dihydropyridines were synthesized and evaluated for pregnancy-interceptive activity in mated hamsters. Our of 24 compounds, 12, 15, 21, 22, 28, and 34 caused a marked reduction in the number of implantations when administered on days 3-8 postcoitum. In an in vitro competition assay, none of the compounds exhibited noticeable binding affinity for uterine progesterone receptors. The results reported here have helped to identify new leads for developing pregnancy-interceptive agents and the active compounds do not seem to elicit their interceptive effect through receptor-mediated inhibition of progesterone action in hamster uterus.

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