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

158642-05-8

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158642-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158642-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,6,4 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 158642-05:
(8*1)+(7*5)+(6*8)+(5*6)+(4*4)+(3*2)+(2*0)+(1*5)=148
148 % 10 = 8
So 158642-05-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H21BrN2/c1-11(2)6-7-16-8-9-19(3)15(16)18-14-10-12(17)4-5-13(14)16/h4-6,10,15,18H,7-9H2,1-3H3/t15-,16-/m0/s1

158642-05-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3aS,8bS)-6-bromo-3-methyl-8b-(3-methylbut-2-enyl)-1,2,3a,4-tetrahydropyrrolo[2,3-b]indole

1.2 Other means of identification

Product number -
Other names (3as,8as)-6-bromo-1-methyl-3a-(3-methylbut-2-en-1-yl)-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole

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:158642-05-8 SDS

158642-05-8Upstream product

158642-05-8Downstream Products

158642-05-8Relevant academic research and scientific papers

First total syntheses of dihydroflustramine C and flustramine E, alkaloids from the marine bryozoan Flustra foliacea

Morales-Ríos, Martha S,Suárez-Castillo, Oscar R,Joseph-Nathan, Pedro

, p. 1479 - 1484 (2002)

We have developed a simple and practical method for providing the common tricyclic skeleton of physostigmine type alkaloids, and demonstrated its utility for indole alkaloid synthesis. Thus, we achieved the first total syntheses of (±)-dihydroflustramine C and (±)-flustramine E, as well as the total syntheses of their debromoanalogues from the corresponding 2-hydroxyindolenines in five steps with 31, 27, 39 and 23% overall yields, respectively. The structures of some intermediates were confirmed by single crystal X-ray diffraction analyses.

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