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15876-37-6

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15876-37-6 Usage

General Description

(2E)-octahydronaphthalen-2(1H)-one oxime, also known as 2-oxime-2-hydronaphthalene, is a chemical compound with the molecular formula C10H13NO. It is an oxime derivative of octahydronaphthalen-2(1H)-one, and it is commonly used in the synthesis of organic compounds and pharmaceuticals. It has a white crystalline appearance and is soluble in organic solvents such as ethanol, acetone, and ether. This chemical has potential applications in the field of organic chemistry, and its properties make it a useful building block for the creation of more complex molecules. Additionally, it is known to have mild stimulant properties and has been studied as a potential treatment for neurological disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 15876-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15876-37:
(7*1)+(6*5)+(5*8)+(4*7)+(3*6)+(2*3)+(1*7)=136
136 % 10 = 6
So 15876-37-6 is a valid CAS Registry Number.

15876-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (NE)-N-(3,4,4a,5,6,7,8,8a-octahydro-1H-naphthalen-2-ylidene)hydroxylamine

1.2 Other means of identification

Product number -
Other names 2-Oxo-trans-decalin-oxim

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:15876-37-6 SDS

15876-37-6Downstream Products

15876-37-6Relevant articles and documents

Reactivite nucleophile des cyclanones: influence de la stereochimie cis/trans en serie bicyclique

Agami, C.,Rizk, T.,Durand, R.,Geneste, P.

, p. 2355 - 2357 (2007/10/02)

The relative reactivities of a number of cis/trans pairs of bicyclic ketones in the 1- and 2-decalone series (2-decalone; 10-methyl-2-decalone; 9-methyl-1-decalone; and 3,10-dimethyl-2-decalone) have been studied for the nucleophilic addition of hydroxylamine in acidic medium.The results obtained as well as the rate constants for neutral or acid catalysed addition always reveal a slight preference for the trans-isomer (x 2.4).This result agrees with the proposal that preferential equatorial attack of a nucleophile is caused by conformational factors related to a steroid non-steroid conformation equilibrium in the cis-isomers.

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