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Pyrrolo[1,2-b]isoxazole, 2-(3,4-dimethoxyphenyl)hexahydro-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86980-84-9

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86980-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86980-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86980-84:
(7*8)+(6*6)+(5*9)+(4*8)+(3*0)+(2*8)+(1*4)=189
189 % 10 = 9
So 86980-84-9 is a valid CAS Registry Number.

86980-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3aR)-2-(3,4-dimethoxyphenyl)-2,3,3a,4,5,6-hexahydropyrrolo[1,2-b][1,2]oxazole

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:86980-84-9 SDS

86980-84-9Relevant academic research and scientific papers

General Synthesis of Phenanthroindolizidine, Phenanthroquinolizidine, and Related Alkaloids: Preparation of (+/-)-Tylophorine, (+/-)-Cryptopleurine, (+/-)-Septicine, and (+/-)-Julandine

Iida, Hideo,Watanabe, Yohya,Tanaka, Masao,Kibayashi, Chihiro

, p. 2412 - 2418 (2007/10/02)

A general synthetic route to the pentacyclic phenanthro class and related indolizidine and quinolizidine alkaloids via β-amino ketone intermediates is reported.The synthesis of tylophorine, cryptopleurine, septicine, and julandine, in racemic forms, has been described.Synthetic steps in the preparation of these alkaloids involve 1,3-dipolar cycloadditions of the cyclic nitrones as a common feature followed by crucial ring closure by aldol reactions and photolyses.

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