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3-Furancarbonitrile, 5-(bromoacetyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133674-68-7

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133674-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133674-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,7 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 133674-68:
(8*1)+(7*3)+(6*3)+(5*6)+(4*7)+(3*4)+(2*6)+(1*8)=137
137 % 10 = 7
So 133674-68-7 is a valid CAS Registry Number.

133674-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-bromoacetyl)furan-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-FURANCARBONITRILE,5-(BROMOACETYL)

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:133674-68-7 SDS

133674-68-7Downstream Products

133674-68-7Relevant academic research and scientific papers

The chemistry of pseudomonic acid part 14. Synthesis and in vivo biological activity of heterocyclyl substituted oxazole derivatives

Broom,Elder,Hannan,Pons,O'Hanlon,Walker,Wilson,Woodall

, p. 1336 - 1344 (2007/10/02)

Semisynthetic analogues of pseudomonic acid A have been prepared containing a heterocyclyl substituted oxazole. Derivatives in which the heterocycle was thiophene, furan, pyridine, or isoxazole showed good antibacterial potency and were further evaluated in vivo. Both pharmacokinetic parameters and oral activity against an experimental intraperitoneal sepsis were superior to results obtained from previously described pseudomonic acid A derivatives.

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