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23454-27-5

(5aS,13aβ)-11aα-(1,1-Dimethyl-2-propenyl)-6aα-hydroxy-2,3,6,6a,11,11a-hexahydro-1H-pyrrolo[1'',2'':4',5']pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-5,13(5aH,13aH)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (5aS,13aβ)-11aα-(1,1-Dimethyl-2-propenyl)-6aα-hydroxy-2,3,6,6a,11,11a-hexahydro-1H-pyrrolo[1'',2'':4',5']pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-5,13(5aH,13aH)-dione

    Cas No: 23454-27-5

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  • (5aS,13aβ)-11aα-(1,1-Dimethyl-2-propenyl)-6aα-hydroxy-2,3,6,6a,11,11a-hexahydro-1H-pyrrolo[1'',2'':4',5']pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-5,13(5aH,13aH)-dione

    Cas No: 23454-27-5

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  • Zhangzhou Sinobioway Peptide Co.,Ltd.
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  • 23454-27-5 Structure

  • Basic information

    1. Product Name: (5aS,13aβ)-11aα-(1,1-Dimethyl-2-propenyl)-6aα-hydroxy-2,3,6,6a,11,11a-hexahydro-1H-pyrrolo[1'',2'':4',5']pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-5,13(5aH,13aH)-dione
    2. Synonyms: (5aS,13aβ)-11aα-(1,1-Dimethyl-2-propenyl)-6aα-hydroxy-2,3,6,6a,11,11a-hexahydro-1H-pyrrolo[1'',2'':4',5']pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-5,13(5aH,13aH)-dione;Brevianamide E
    3. CAS NO:23454-27-5
    4. Molecular Formula: C21H25N3O3
    5. Molecular Weight: 367.4415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23454-27-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 598°Cat760mmHg
    3. Flash Point: 315.5°C
    4. Appearance: /
    5. Density: 1.36g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (5aS,13aβ)-11aα-(1,1-Dimethyl-2-propenyl)-6aα-hydroxy-2,3,6,6a,11,11a-hexahydro-1H-pyrrolo[1'',2'':4',5']pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-5,13(5aH,13aH)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5aS,13aβ)-11aα-(1,1-Dimethyl-2-propenyl)-6aα-hydroxy-2,3,6,6a,11,11a-hexahydro-1H-pyrrolo[1'',2'':4',5']pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-5,13(5aH,13aH)-dione(23454-27-5)
    11. EPA Substance Registry System: (5aS,13aβ)-11aα-(1,1-Dimethyl-2-propenyl)-6aα-hydroxy-2,3,6,6a,11,11a-hexahydro-1H-pyrrolo[1'',2'':4',5']pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-5,13(5aH,13aH)-dione(23454-27-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 23454-27-5(Hazardous Substances Data)

23454-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23454-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,5 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23454-27:
(7*2)+(6*3)+(5*4)+(4*5)+(3*4)+(2*2)+(1*7)=95
95 % 10 = 5
So 23454-27-5 is a valid CAS Registry Number.

23454-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6a-hydroxy-11a-(2-methylbut-3-en-2-yl)-1,2,3,6,6a,11,11a,13a-octahydro-13H-pyrrolo[1'',2'':4',5']pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-5,13(5aH)-dione

1.2 Other means of identification

Product number -
Other names -

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

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More Details:23454-27-5 SDS

23454-27-5Downstream Products

23454-27-5Relevant articles and documents

Stereoselective synthesis of brevianamide e

Zhao, Liang,May, Jonathan P.,Huang, Jack,Perrin, David M.

supporting information; experimental part, p. 90 - 93 (2012/02/15)

The hydroxypyrroloindolenine (Hpi) motif forms the fundamental core of the pentacyclic natural product, brevianamide E, the concise stereoselective synthesis of which, via oxidative cyclization, is described.

Studies on the Syntheses of Heterocyclic Compounds. Part 876. The Chiral Total Synthesis of Brevianamide E and Deoxybrevianamide E

Kametani, Tetsuji,Kanaya, Naoaki,Ihara, Masataka

, p. 959 - 963 (2007/10/02)

The chiral total synthesis of brevianamide E (1) and deoxybrevianamide E (2) starting from L-proline is described.Condensation of 2-(1,1,dimethylallyl)-3-dimethylaminomethylindole (3) and (-)-methyl 1,4-dioxoperhydropyrrolopyrazine-3-carboxylate (7

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