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19860-71-0

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19860-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19860-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,6 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19860-71:
(7*1)+(6*9)+(5*8)+(4*6)+(3*0)+(2*7)+(1*1)=140
140 % 10 = 0
So 19860-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c1-4-5-6-9(10)7-8(2)3/h7H,4-6H2,1-3H3

19860-71-0SDS

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 2-methyloct-2-en-4-one

1.2 Other means of identification

Product number -
Other names 2-Octen-4-one,2-methyl

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:19860-71-0 SDS

19860-71-0Downstream Products

19860-71-0Relevant articles and documents

New preparation of stereodefined α,α-unsaturated ketones by carbomagnesiation of α-allenyl ketones

Chinkov, Nicka,Morlender-Vais, Natalia,Marek, Ilan

, p. 6009 - 6010 (2002)

The addition of several alkylmagnesium halides to an α-allenyl ketone leads to the corresponding α,β-unsaturated ketones as single geometrical isomers. A π-chelation between the metal and the unsaturation is proposed to explain the steric outcome of this reaction.

Domino gold-catalyzed rearrangement and fluorination of propargyl acetates

De Haro, Teresa,Nevado, Cristina

supporting information; scheme or table, p. 248 - 249 (2011/02/23)

A combination of IPrAuNTf2 as catalyst in the presence of Selectfluor has been successfully used for the high yielding synthesis of α-fluoroenones via 1,3-acyloxy rearrangement of propargyl acetates followed by Csp2-F bond formation,

4,5 Dihydro-(1H)-Pyrazole Derivatives as Cannabinoid CB1 Receptor Modulators

-

Page/Page column 12, (2009/01/24)

The invention is directed to 4,5-dihydro-(1H)-pyrazole (pyrazoline) derivatives as cannabinoid CB1 receptor modulators, to pharmaceutical compositions comprising these compounds, to methods for their syntheses, to methods for preparing novel intermediates useful for their syntheses, and to methods for preparing compositions. The invention also relates to the uses of compounds and compositions administered to patients to achieve a therapeutic effect in multiple sclerosis, traumatic brain injury, pain including chronic pain, neuropathic pain, acute pain and inflammatory pain, osteoporosis, appetite disorders, epilepsy, Alzheimer's disease, Tourette's syndrome, cerebral ischaemia, emesis, nausea, and gastrointestinal disorders. Compounds of the present disclosure are directed to formula (I): wherein the substituents have the definitions given in the specification.

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