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65284-99-3

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65284-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65284-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,8 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65284-99:
(7*6)+(6*5)+(5*2)+(4*8)+(3*4)+(2*9)+(1*9)=153
153 % 10 = 3
So 65284-99-3 is a valid CAS Registry Number.

65284-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Nb-benzyl-1,2,3,3a,4,5-hexahydrocanthin-6-one

1.2 Other means of identification

Product number -
Other names 3-benzyl-1,2,3,3a,4,5-hexahydro-indolo[3,2,1-de][1,5]naphthyridin-6-one

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:65284-99-3 SDS

65284-99-3Relevant articles and documents

Cantffln - 6 - quaternary ammonium salt and its preparation method and application

-

Paragraph 0033; 0036; 0037, (2017/12/02)

The invention relates to a canthium dicoccum-6-one quaternary ammonium salt and a preparation method and an application thereof. The structural formula of the compound is shown in a formula (1) in the specification, wherein R is ethyl, propyl, isopropyl, allyl, normal-butyl, isobutyl, normal-amyl, normal-octyl, unsubstituted benzyl or substituted benzyl substituted by a hydrogen atom, methyl, bromomethyl, trifluoromethyl, benzyloxyl, a fluorine atom or a chlorine atom; X is chlorine, bromine or iodine. The application is that of the compound for preparing antibacterial drugs.

An improved synthesis of canthin-6-one

Czerwinski, Kevin M.,Zificsak, Craig A.,Stevens, John,Oberbeck, Melissa,Randlett, Christopher,King, Melissa,Mennen, Steve

, p. 1225 - 1231 (2007/10/03)

An improved route has been devised which provides canthin-6-one in the highest yield from tryptamine to date. Tryptamine is converted to Nb-benzyltryptamine via reaction with benzoylchloride and reduction using LAH. Pictet-Spengler condensation with 2-ketoglutaric acid, removal of the protecting group by CTH, and aromatization with MnO2 affords canthin-6-one in 48% overall yield.

A New Synthesisof(+/-)Trypargine

Shimizu, Masato,Ishikawa, Masayuki,Komoda, Yasuo,Matsubara, Yukimi,Nakajima, Terumi

, p. 4529 - 4533 (2007/10/02)

A new route for the synthesis of (+/-)-trypargine (I) is described.The Pictet-Spengler reaction of Nb-benzyltryptamine with α-ketoglutaric acid was carried out in aprotic media to afford the key intermediate, 2-benzyl-1,2,3,3-tetrahydro-9H-pyri

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