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6-ETHOXY-2-TETRALONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69788-78-9

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69788-78-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69788-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,8 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69788-78:
(7*6)+(6*9)+(5*7)+(4*8)+(3*8)+(2*7)+(1*8)=209
209 % 10 = 9
So 69788-78-9 is a valid CAS Registry Number.

69788-78-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethoxy-3,4-dihydro-2(1H)-naphthalenone

1.2 Other means of identification

Product number -
Other names 6-ethoxy-2-tetralone

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:69788-78-9 SDS

69788-78-9Relevant academic research and scientific papers

Substituted pyridines/pyrimidines, their preparation and their use as pesticides

-

, (2008/06/13)

The present invention relates to novel substituted pyridines/pyrimidines of the formula I where A is CH or N; X is NH, O or S(O)qwhere q is 0, 1 or 2; Y1, Y2and Y3independently of one another are a group of the

Spasmolytic Agents. 2. 1,2,3,4-Tetrahydro-2-naphthylamine Derivatives

Kanao, Munefumi,Hashizume, Takeshi,Ichikawa, Yoshifumi,Irie, Kiyoshi,Isoda, Sumiro

, p. 1358 - 1363 (2007/10/02)

N--1,2,3,4-tetrahydro-2-naphthylamine derivatives were synthesized from 1,2,3,4-tetrahydro-2-naphthylamines evaluated for their spasmolytic activity.Some of these compounds showed a nerve-selective effect on colon rather than stomach in anesthetized dogs and were found to be equal to or more active than the reference drug (mebeverine).The biological data have indicated some structure-activity relationships.Among these compounds, N-ethyl-N-hexyl>-1,2,3,4-tetrahydro-6-methoxy-2-naphthylamine hydrochloride (63) was found to be the most active spasmolytic agent.

2-Aminotetralin derivatives and process for producing the same

-

, (2008/06/13)

Compounds, which have antispasmodic effects, represented by the following formula (I) STR1 wherein R 1 and R 2, which may be the same or different, each represents a hydrogen atom, an alkoxy group or, when taken together, R 1 and R 2 represent an alkylenedioxy group; R 3 represents a hydrogen atom, an alkyl group or a cycloalkyl group; R 4, R 5 and R 6, which may be the same or different, each represents a hydrogen atom, an alkoxy group, an alkyl group, a halogen atom, a hydroxyl group or, when two of R 4, R 5 and R 6 are taken together, they represent an alkylenedioxy group; and A represents a straight or branched chain alkylene group having 2 to 10 carbon atoms or an alkylene group having 2 to 10 carbon atoms and interrupted with an oxygen atom forming an ether bond therein, and the therapeutically useful acid-addition salts thereof; and a process for producing the same.

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