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18800-78-7

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  • Carbamic acid,[(1S)-4-amino-1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-4-oxobutyl]-,1,1-dimethylethyl ester (9CI)

    Cas No: 18800-78-7

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  • Carbamic acid,[(1S)-4-amino-1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-4-oxobutyl]-,1,1-dimethylethyl ester (9CI) cas 18800-78-7

    Cas No: 18800-78-7

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18800-78-7 Usage

Chemical Properties

White to off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 18800-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,0 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18800-78:
(7*1)+(6*8)+(5*8)+(4*0)+(3*0)+(2*7)+(1*8)=117
117 % 10 = 7
So 18800-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H21N3O7/c1-14(2,3)23-13(22)16-8(4-5-9(15)18)12(21)24-17-10(19)6-7-11(17)20/h8H,4-7H2,1-3H3,(H2,15,18)(H,16,22)

18800-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-GLN-OSU

1.2 Other means of identification

Product number -
Other names N-tert-Butoxycarbonyl-L-glutamine-N-hydroxysuccinimide est

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:18800-78-7 SDS

18800-78-7Relevant articles and documents

Dissecting modular synthases through inhibition: A complementary chemical and genetic approach

Vickery, Christopher R.,McCulloch, Ian P.,Sonnenschein, Eva C.,Beld, Joris,Noel, Joseph P.,Burkart, Michael D.

, (2020)

Modular synthases, such as fatty acid, polyketide, and non-ribosomal peptide synthases (NRPSs), are sophisticated machineries essential in both primary and secondary metabolism. Various techniques have been developed to understand their genetic background and enzymatic abilities. However, uncovering the actual biosynthetic pathways remains challenging. Herein, we demonstrate a pipeline to study an assembly line synthase by interrogating the enzymatic function of each individual enzymatic domain of BpsA, a NRPS that produces the blue 3,3′-bipyridyl pigment indigoidine. Specific inhibitors for each biosynthetic domain of BpsA were obtained or synthesized, and the enzymatic performance of BpsA upon addition of each inhibitor was monitored by pigment development in vitro and in living bacteria. The results were verified using genetic mutants to inactivate each domain. Finally, the results complemented the currently proposed biosynthetic pathway of BpsA.

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