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454451-28-6

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454451-28-6 Usage

Uses

tert-Butyl Azepan-4-ylcarbamate is used in preparation of cytosine derivatives as antimicrobial agents for the treatment of bacterial infections.

Check Digit Verification of cas no

The CAS Registry Mumber 454451-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,4,5 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 454451-28:
(8*4)+(7*5)+(6*4)+(5*4)+(4*5)+(3*1)+(2*2)+(1*8)=146
146 % 10 = 6
So 454451-28-6 is a valid CAS Registry Number.

454451-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl azepan-4-ylcarbamate

1.2 Other means of identification

Product number -
Other names tert-butyl N-(azepan-4-yl)carbamate

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:454451-28-6 SDS

454451-28-6Downstream Products

454451-28-6Relevant articles and documents

Side chain SAR of bicyclic β-lactamase inhibitors (BLIs). 2. N-Alkylated and open chain analogs of MK-8712

Chen, Helen,Blizzard, Timothy A.,Kim, Seongkon,Wu, Jane,Young, Katherine,Park, Young-Whan,Ogawa, Aimie M.,Raghoobar, Susan,Painter, Ronald E.,Wisniewski, Doug,Hairston, Nichelle,Fitzgerald, Paula,Sharma, Nandini,Scapin, Giovanna,Lu, Jun,Hermes, Jeff,Hammond, Milton L.

scheme or table, p. 4267 - 4270 (2011/08/06)

The bridged monobactam β-lactamase inhibitor MK-8712 (1) effectively inhibits class C β-lactamases. Side chain N-alkylated and ring-opened analogs of 1 were prepared and evaluated for combination with imipenem to overcome class C β-lactamase mediated resi

Xanthine derivatives, the preparation thereof and their use as pharmaceutical compositions

-

, (2008/06/13)

The present invention relates to substituted xanthines of general formula wherein R1 to R4 are defined as in claim 1, the tautomers and the stereoisomers thereof, mixtures thereof, the prodrugs and the salts thereof which have valuable pharmacological properties, particularly an inhibiting effect on the activity of the enzyme dipeptidylpeptidase-IV (DPP-IV).

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