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106040-03-3

3H-Pyrrolizin-3-one, hexahydro-5-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106040-03-3

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106040-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106040-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,4 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106040-03:
(8*1)+(7*0)+(6*6)+(5*0)+(4*4)+(3*0)+(2*0)+(1*3)=63
63 % 10 = 3
So 106040-03-3 is a valid CAS Registry Number.

106040-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name hexahydro-5-hydroxy-3H-pyrrolizin-3-one

1.2 Other means of identification

Product number -
Other names 5-Hydroxy-hexahydro-pyrrolizin-3-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:106040-03-3 SDS

106040-03-3Relevant articles and documents

Reaction of Novel Imide Reducing Reagents with Pyrrolizidinediones

Thomas, Edward W.,Rynbrandt, Ronald H.,Zimmermann, David C.,Bell, Larry T.,Muchmore, Christine R.,Yankee, Ernest W.

, p. 4535 - 4543 (1989)

The reduction of pyrrolizidinediones 4a and 4b with (i-Bu)2AlH and LiBHEt3 affords the corresponding hexahydro-5-hydroxy-3H-pyrrolizin-3-ones 8a and 8b in good yield.LiBHEt3 also reduces N-methylglutarimide (18) in 53percent yield.The combination of NaBH4/MeOH/Ac2O/CH2Cl2 selectivity reduces an imide in the presence of an ester.Hexahydro-5-(methylthio)-3H-pyrrolizin-3-ones are products of the NaBH4 reduction of pyrrolizidinediones in MeSH/CH2Cl2/Ac2O.The reduction products, thioethers (5a-c) and lactamols (8a-c), are intermediates in the synthesis of pyrrolizinones 1a-c.

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