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152302-33-5

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152302-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152302-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,3,0 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 152302-33:
(8*1)+(7*5)+(6*2)+(5*3)+(4*0)+(3*2)+(2*3)+(1*3)=85
85 % 10 = 5
So 152302-33-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H19NO/c19-17(15-8-4-9-15)18-12-11-14-7-3-6-13-5-1-2-10-16(13)14/h1-3,5-7,10,15H,4,8-9,11-12H2,(H,18,19)

152302-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-naphthalen-1-ylethyl)cyclobutanecarboxamide

1.2 Other means of identification

Product number -
Other names N-(2-(1-Naphthalenyl)ethyl)cyclobutanecarboxamide

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:152302-33-5 SDS

152302-33-5Downstream Products

152302-33-5Relevant articles and documents

Synthesis and structure - Activity relationships of novel naphthalenic and bioisosteric related amidic derivatives as melatonin receptor ligands

Leclerc, Veronique,Fourmaintraux, Eric,Depreux, Patrick,Lesieur, Daniel,Morgan, Peter,Howell, H. Edward,Renard, Pierre,Caignard, Daniel-Henri,Pfeiffer, Bruno,Delagrange, Philippe,Guardiola-Lemaitre, Beatrice,Andrieux, Jean

, p. 1875 - 1887 (1998)

A previous paper reported the synthesis of melatonin receptor ligands. In order to complete the structure-activity relationships and to obtain antagonists to the melatonin receptor, a new series of naphthalenic analogues of melatonin have been synthesized

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