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5(1H)-Indolizinone,2,3,8,8a-tetrahydro-8-hydroxy-8-methyl-,(8S,8aS)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

705927-10-2

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705927-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 705927-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,5,9,2 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 705927-10:
(8*7)+(7*0)+(6*5)+(5*9)+(4*2)+(3*7)+(2*1)+(1*0)=162
162 % 10 = 2
So 705927-10-2 is a valid CAS Registry Number.

705927-10-2SDS

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 (8S,8aS)-8-hydroxy-8-methyl-2,3,8,8a-tetrahydro-1H-indolizin-5-one

1.2 Other means of identification

Product number -
Other names (8S,8aS)-8-Hydroxy-8-methyl-2,3,8,8a-tetrahydro-1H-indolizin-5-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:705927-10-2 SDS

705927-10-2Downstream Products

705927-10-2Relevant academic research and scientific papers

Rapid stereoselective access to key pumiliotoxin precursors from a common intermediate

O'Mahony, Gavin,Nieuwenhuyzen, Mark,Armstrong, Paul,Stevenson, Paul J.

, p. 3968 - 3971 (2004)

Epoxidation and dihydroxylation of 8-methyl-2,3,6,8a-tetrahydro-1H-indolizin-5-one proceeded from the concave face with good selectivity and gave advanced precursors for pumiliotoxin and allopumiliotoxin synthesis, respectively. The origin of the selectivity is believed to be stereoelectronic in nature and allows rapid entry to three different pumiliotoxin classes from a common intermediate.

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