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3H-Pyrrolizin-3-one, hexahydro-7a-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104885-96-3

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104885-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104885-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,8 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104885-96:
(8*1)+(7*0)+(6*4)+(5*8)+(4*8)+(3*5)+(2*9)+(1*6)=143
143 % 10 = 3
So 104885-96-3 is a valid CAS Registry Number.

104885-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-hydroxy-2,5,6,7-tetrahydro-1H-pyrrolizin-3-one

1.2 Other means of identification

Product number -
Other names 7a-hydroxy-hexahydro-3H-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:104885-96-3 SDS

104885-96-3Downstream Products

104885-96-3Relevant academic research and scientific papers

Reductive cyclization of N-iodoalkyl cyclic imides to nitrogen-fused polycyclic amides induced by samarium diiodide

Ha, Deok-Chan,Yun, Chang-Soo,Yu, Eunsun

, p. 2577 - 2580 (1996)

SmI2-promoted cyclizations of cyclic imides having 3-iodopropyl or 4-iodobutyl groups on the imide nitrogen have been studied for construction of nitrogen-fused polycyclic amides.

Syntheses of Pyrrolizidines,III

Flitsch, Wilhelm,Hampel, Klaus

, p. 387 - 390 (2007/10/02)

The pyrrolizindinone 2a was obtained from 1-bromo-3-(triphenylphosphoranylidene)-2-propanone and the anion of succinimide; reaction with the cyclopropylphosphonium bromide 7 gave the hydroxypyrrolizidinone 9.Functionalization of the "hydroxypyrrole" 2 yielded the derivatives 3-6.By regioselective acetoxylation of 9 (to yield 14) and subsequent Vilsmeier formylation the acetoxypyrrolizinecarbaldehyde 15 was obtined.

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