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4-(2-Amino-1H-imidazol-4-yl)-2,3-dibromo-6,7-dihydropyrrolo[2,3-c]azepin-8(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99102-22-4

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99102-22-4 Usage

Uses

Stevensine is a dibrominated alkaloid deterrant of predatory fishes.

Check Digit Verification of cas no

The CAS Registry Mumber 99102-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,1,0 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99102-22:
(7*9)+(6*9)+(5*1)+(4*0)+(3*2)+(2*2)+(1*2)=134
134 % 10 = 4
So 99102-22-4 is a valid CAS Registry Number.

99102-22-4SDS

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 4-(2-amino-1H-imidazol-5-yl)-2,3-dibromo-6,7-dihydro-1H-pyrrolo[2,3-c]azepin-8-one

1.2 Other means of identification

Product number -
Other names stevensine

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:99102-22-4 SDS

99102-22-4Downstream Products

99102-22-4Relevant academic research and scientific papers

Transbromination of brominated pyrrole and imidazole derivatives: Synthesis of the C11N5 marine alkaloid stevensine

Xu, Ying-Zi,Yakushijin, Kenichi,Horne, David A.

, p. 8121 - 8124 (2007/10/03)

The marine sponge alkaloid stevensine (3) has been synthesized from the related C11N5 alkaloid, hymenin (1). The key transformation involves a regioselective protodebromination/transbromination event of 4'-bromohymenin (2) to install the olefin in 3. Such processes are seldom used for synthetic purposes but appear to be highly applicable to the C11N5 family of marine alkaloids.

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