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108354-12-7

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108354-12-7 Usage

Definition

ChEBI: An A-type aurachin that is quinoline N-oxide which is substituted by a methyl group at position 2, a hydroxy group at position 3, and a triprenyl group at position 4.

Check Digit Verification of cas no

The CAS Registry Mumber 108354-12-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,5 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 108354-12:
(8*1)+(7*0)+(6*8)+(5*3)+(4*5)+(3*4)+(2*1)+(1*2)=107
107 % 10 = 7
So 108354-12-7 is a valid CAS Registry Number.
InChI:InChI=1/C25H33NO2/c1-18(2)10-8-11-19(3)12-9-13-20(4)16-17-23-22-14-6-7-15-24(22)26(28)21(5)25(23)27/h6-7,10,12,14-16,27H,8-9,11,13,17H2,1-5H3/b19-12+,20-16+

108354-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-oxido-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]quinolin-1-ium-3-ol

1.2 Other means of identification

Product number -
Other names Aurachin B

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:108354-12-7 SDS

108354-12-7Upstream product

108354-12-7Downstream Products

108354-12-7Relevant articles and documents

A semipinacol rearrangement directed by an enzymatic system featuring dual-function FAD-dependent monooxygenase

Katsuyama, Yohei,Harmrolfs, Kirsten,Pistorius, Dominik,Li, Yanyan,Müller, Rolf

, p. 9437 - 9440 (2012)

The biosynthesis of aurachins includes the intriguing migration of the prenyl group by a pinacol-type rearrangement. In vitro analysis of AuaGH revealed that these enzymes catalyze epoxidation coupled with semipinacol rearrangement (see scheme) and ketoreduction. Thus, the AuaGH system was revealed to be a novel enzymatic system for establishing semipinacol rearrangements.

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