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Methyl 6-methoxy-4-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate is a complex organic compound with the molecular formula C12H12O4. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, and features a methyl ester group, a methoxy group, and a carbonyl group. methyl 6-methoxy-4-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate is characterized by its 1,2,3,4-tetrahydro structure, which means that one of the double bonds in the naphthalene ring has been reduced to a single bond, and it has four hydrogen atoms attached to the carbon atoms of the ring. The 6-methoxy group indicates the presence of a methoxy (-OCH3) substituent at the 6th position of the naphthalene ring, while the 4-oxo group signifies a carbonyl (C=O) group at the 4th position. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

6271-18-7

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6271-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6271-18-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6271-18:
(6*6)+(5*2)+(4*7)+(3*1)+(2*1)+(1*8)=87
87 % 10 = 7
So 6271-18-7 is a valid CAS Registry Number.

6271-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Methoxy-4-oxo-1,2,3,4-tetrahydro-[2]naphthoesaeure-methylester

1.2 Other means of identification

Product number -
Other names 6-methoxy-4-oxo-1,2,3,4-tetrahydro-[2]naphthoic acid methyl 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:6271-18-7 SDS

6271-18-7Downstream Products

6271-18-7Relevant academic research and scientific papers

Kinetic resolution of 3-hydroxymethylbenzocycloalkanols by selective asymmetric hydrogen-transfer oxidation

Caro, Yolanda,Torrado, Maria,Masaguer, Christian F.,Ravina, Enrique

, p. 3689 - 3696 (2007/10/03)

Kinetic resolution of 3-hydroxymethylbenzocycloalkanols was performed by selective asymmetric hydrogen-transfer oxidation using the Ru(II)-(S,S)-TsDPEN catalyst. Thus, several 3-hydroxymethyl-1-tetralols 7a-d afforded (1R,3R)-3-hydroxymethyl-1-tetralols (

Synthesis and analgetic activity of some benzomorphan analogues

Kometani,Shiotani

, p. 1105 - 1110 (2007/10/06)

The benzomorphan analogues, 8-hydroxy-3-methyl-2,3,4,5-etrahydro-1,4-methano-1H-3-benzazepine (1), 8-hydroxy-2-methyl-2,3,4,5-tetrahydro-1,4-methano-1H-2-benzazepine (2), 9-hydroxy-2-methyl-1,2,3,4,5,6-hexa-hydro-1,5-methano-2-benzazocine (3), and 10-hydr

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