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CYCLOPIAZONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83136-88-3

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83136-88-3 Usage

Uses

Cyclopiazonic Acid is an inhibitor of endoplasmic reticulum Ca2+-ATPase.

Check Digit Verification of cas no

The CAS Registry Mumber 83136-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,3 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83136-88:
(7*8)+(6*3)+(5*1)+(4*3)+(3*6)+(2*8)+(1*8)=133
133 % 10 = 3
So 83136-88-3 is a valid CAS Registry Number.

83136-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name α-cyclopiazonic acid

1.2 Other means of identification

Product number -
Other names alpha-cyclopiazonic acid

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:83136-88-3 SDS

83136-88-3Downstream Products

83136-88-3Relevant academic research and scientific papers

A total synthesis of (±)-α-cyclopiazonic acid using a cationic cascade

Haskins, Charlotte M.,Knight, David W.

, p. 3162 - 3164 (2008/02/12)

The indolic terpene alkaloid α-cyclopiazonic acid 1 has been prepared in 11 steps from indole-4-methanol 6; the key step is a carbocationic cascade, terminated by a 4-nitrosulfonamide group and initiated by benzylic carbocation formation directly from the

TOTAL SYNTHESIS OF (+/-)-α-CYCLOPIAZONIC ACID

Muratake, Hideaki,Natsume, Mitsutaka

, p. 1111 - 1117 (2007/10/02)

(+/-)-α-Cyclopiazonic acid (2) was synthesized from 1-methoxycarbonyl-4-(3-oxo-1-butyl)indole (1) by way of 17, 18, and 19 using a reaction of MeLi with a pyrroline derivative 33 in the presence of BF3*Et2O.

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