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1487-99-6

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1487-99-6 Usage

Structure

Seven-membered cyclic ether with two methyl groups attached to the second and seventh carbon atoms

Usage

Building block for organic synthesis, used in the production of various organic molecules and pharmaceuticals

Properties

Antibacterial and antifungal, potential candidate for the development of new antimicrobial agents
Volatile compound with a fruity odor
Used in the flavor and fragrance industry to impart a pleasant scent to various products

Check Digit Verification of cas no

The CAS Registry Mumber 1487-99-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1487-99:
(6*1)+(5*4)+(4*8)+(3*7)+(2*9)+(1*9)=106
106 % 10 = 6
So 1487-99-6 is a valid CAS Registry Number.

1487-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dimethyloxepine

1.2 Other means of identification

Product number -
Other names Oxepin,2,7-dimethyl

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:1487-99-6 SDS

1487-99-6Relevant articles and documents

Direct Observation of an Oxepin from a Bacterial Cytochrome P450-Catalyzed Oxidation

Stok, Jeanette E.,Chow, Sharon,Krenske, Elizabeth H.,Farfan Soto, Clementina,Matyas, Csongor,Poirier, Raymond A.,Williams, Craig M.,De Voss, James J.

, p. 4408 - 4412 (2016)

The cytochromes P450 are hemoproteins that catalyze a range of oxidative C-H functionalization reactions, including aliphatic and aromatic hydroxylation. These transformations are important in a range of biological contexts, including biosynthesis and xen

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