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70521-94-7

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70521-94-7 Usage

Occurrence

Sesbania drummondii yields this spiro alkaloid. The base yields colourless rods from EtOH and is dextrorotatory with a specific rotation of [α]D23 + 14.6° (c 0.56, MeOH).

Check Digit Verification of cas no

The CAS Registry Mumber 70521-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,2 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70521-94:
(7*7)+(6*0)+(5*5)+(4*2)+(3*1)+(2*9)+(1*4)=107
107 % 10 = 7
So 70521-94-7 is a valid CAS Registry Number.

70521-94-7SDS

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 3'-hydroxyspiro[2,7-naphthyridine-4,1'-cyclopentane]-1,3-dione

1.2 Other means of identification

Product number -
Other names 3-hydroxy-spiro[cyclopentane-1,4'-[2,7]naphthyridine]-1',3'-dione

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:70521-94-7 SDS

70521-94-7Upstream product

70521-94-7Relevant articles and documents

Stereoselective reactions XIII. Total synthesis of (+)-sesbanine by a highly stereoselective cycloannelation reaction

Tomioka,Koga

, p. 4351 - 4355 (2007/10/02)

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AN EFFICIENT CHIRAL SYNTHESIS OF (+)-SESBANINE

Tomioka, Kiyoshi,Koga, Kenji

, p. 2321 - 2324 (2007/10/02)

(+)-Sesbanine was effectively synthesized from 4-methylnicotinonitrile and 1-malic acid.

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