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2-Pyrrolidinone,5-ethenyl-4-hydroxy-1-(1-methylethyl)-,(4S,5R)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

608525-74-2

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608525-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 608525-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,8,5,2 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 608525-74:
(8*6)+(7*0)+(6*8)+(5*5)+(4*2)+(3*5)+(2*7)+(1*4)=162
162 % 10 = 2
So 608525-74-2 is a valid CAS Registry Number.

608525-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-1-isopropyl-5-vinylpyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names (4S,5R)-4-Hydroxy-1-isopropyl-5-vinyl-pyrrolidin-2-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:608525-74-2 SDS

608525-74-2Downstream Products

608525-74-2Relevant academic research and scientific papers

Concise Formal Synthesis of (-)-Peduncularine via Ring-Closing Metathesis

Washburn, David G.,Heidebrecht Jr., Richard W.,Martin, Stephen F.

, p. 3523 - 3525 (2003)

Equation presented. A synthesis of the 6-aza[3.2.1]bicyclooctene (-)-2 has been completed by a short sequence of reactions that required only six operations from (S)-malic acid and featured a novel ring-closing metathesis to form the bridged bicyclic ring. Because 2 was previously converted into (-)-peduncularine (1), its preparation constitutes a formal enantioselective synthesis of 1.

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