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83-95-4

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83-95-4 Usage

Uses

Skimmianin is an antimicrobial agent extracted from bark Helietta Apiculata Benth (Rutaceae).

Check Digit Verification of cas no

The CAS Registry Mumber 83-95-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83-95:
(4*8)+(3*3)+(2*9)+(1*5)=64
64 % 10 = 4
So 83-95-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO4/c1-16-10-5-4-8-11(13(10)18-3)15-14-9(6-7-19-14)12(8)17-2/h4-7H,1-3H3

83-95-4SDS

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 4,7,8-trimethoxyfuro[2,3-b]quinoline

1.2 Other means of identification

Product number -
Other names skimmiamine

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:83-95-4 SDS

83-95-4Relevant articles and documents

STRUCTURE OF PERFAMINE

Razakova, D. M.,Bessonova, I. A.,Yunusov, S. Yu.

, p. 245 (1983)

-

cis-dihydrodiol, arene oxide and phenol metabolites of dictamnine: Key intermediates in the biodegradation and biosynthesis of furoquinoline alkaloids

Boyd, Derek R.,Sharma, Narain D.,O'Dowd, Colin R.,Carroll, Jonathan G.,Loke, Pui L.,Allen, Christopher C. R.

, p. 3989 - 3991 (2007/10/03)

Biotransformation of the parent furoquinoline alkaloid dictamnine and its 4-chlorofuroquinoline precursor, using the B8/ 36 bacterial mutant strain of Sphingomonas yanoikuyae, yielded, via biphenyl dioxygenase-catalysed dihydroxylation, the first isolable alkaloid cis-dihydrodiol metabolites; these metabolites were used in the chemoenzymatic synthesis of postulated arene oxide and phenol intermediates, and a range of derived furoquinoline alkaloids. The Royal Society of Chemistry 2005.

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