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(3S)-3-[[2-(1,1-Dimethyl-2-propenyl)-1H-indol-3-yl]methyl]-6,7-dihydropyrrolo[1,2-a]pyrazine-1,4(2H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41222-64-4

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41222-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41222-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,2 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41222-64:
(7*4)+(6*1)+(5*2)+(4*2)+(3*2)+(2*6)+(1*4)=74
74 % 10 = 4
So 41222-64-4 is a valid CAS Registry Number.

41222-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 12,13-dehydroprolyl-2-(1,1-dimethylallyltryptophyl)diketopiperazine

1.2 Other means of identification

Product number -
Other names 3-[2-(1,1-dimethyl-allyl)-indol-3-ylmethyl]-2,3,6,7-tetrahydro-pyrrolo[1,2-a]pyrazine-1,4-dione

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:41222-64-4 SDS

41222-64-4Downstream Products

41222-64-4Relevant academic research and scientific papers

Total synthesis of brevianamide A

Godfrey, Robert C.,Green, Nicholas J.,Nichol, Gary S.,Lawrence, Andrew L.

, p. 615 - 619 (2020)

The fungal-derived bicyclo[2.2.2]diazaoctane alkaloids are of interest to the scientific community for their potent and varied biological activities. Within this large and diverse family of natural products, the insecticidal metabolite (+)-brevianamide A is particularly noteworthy for its synthetic intractability and inexplicable biogenesis. Despite five decades of research, this alkaloid has remained an elusive target for chemical synthesis due to insurmountable issues of reactivity and selectivity associated with all previously explored strategies. We herein report the chemical synthesis of (+)-brevianamide A (seven steps, 7.2% overall yield, 750 mg scale), which involves a bioinspired cascade transformation of the linearly fused (?)-dehydrobrevianamide E into the topologically complex bridged-spiro-fused structure of (+)-brevianamide A. [Figure not available: see fulltext.]

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