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36101-54-9

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36101-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36101-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,0 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36101-54:
(7*3)+(6*6)+(5*1)+(4*0)+(3*1)+(2*5)+(1*4)=79
79 % 10 = 9
So 36101-54-9 is a valid CAS Registry Number.

36101-54-9SDS

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 PEGANOLE

1.2 Other means of identification

Product number -
Other names -

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:36101-54-9 SDS

36101-54-9Downstream Products

36101-54-9Relevant academic research and scientific papers

Direction of bromination and nitration of deoxypeganine and its hydrochloride using HPTLC. Synthesis of 6-bromo(nitro)-, 6,8- dinitrodeoxyvasicinones, 6-nitro(bromo)-, 6,8-dinitrodeoxypeganines, and 6H(bromo)peganols

Shakhidoyatov,Mukarramov,Utaeva

experimental part, p. 625 - 629 (2009/04/07)

The reaction of deoxypeganine (DOP) (1) and its hydrochloride (DOP?HCl) (2) with N-bromosuccinimide and a nitrating mixture was studied. It was found that bromination of DOP occurred at C-4 and the aromatic ring. Nitration of DOP?HCl produced either 6-nitro- or 6,8-dinitro-deoxypeganines and 6-nitrodeoxyvasicinone or their mixture in various ratios depending on the substrate:nitrating mixture ratio. 6Hand 6-Br-deoxypeganines were transformed into the 4-hydroxy derivatives, 6H(Br) peganols or deoxyvasicinones. A method for qualitative and quantitative analysis of the pure compounds and the mixture of reaction products using HPTLC was developed. Springer Science+Business Media, Inc. 2008.

Alkaloids of Nitraria komarovii. Structures of komarin and peganol-N-oxide

Tulyaganov,Makhmudov

, p. 76 - 78 (2007/10/03)

Two alkaloids are isolated from the aerial portions of Nitraria komarovii. Their structures are determined using spectral data and chemical transformations.

ALKALOIDS OF Peganum harmala. UNUSUAL REACTION OF PEGANINE AND VASICINONE

Telezhenetskaya, M. V.,D'yakonov, A. L.

, p. 471 - 474 (2007/10/02)

A number of derivatives of peganine and vasicinone have been obtained: 4-hydroxy-9-O-methylpeganine, isodihydrovasicinone, and 9-methoxy-, 9-phenoxy-, and 9,9-dichlorodeoxyvasicinones.An unusual ease of reduction of vasicinone and of 9-chlorodeoxyvasicinone has been found.An introduction of a hydroxy group into position 4 of a dihydroquinazoline alkaloid with the aid of sodium hydride has been detected.

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