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1198-67-0

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1198-67-0 Usage

Molecular class

Pyrrole carboxylic acid derivative

Structure

Methyl ester derivative of 3,4,5-tribromo-1H-pyrrole-2-carboxylic acid

Usage

Organic synthesis and pharmaceutical research

Biological activities

Potential biological activities

Intermediate

Used as an intermediate in the production of various pharmaceuticals and agrochemicals

Handling precautions

Potential hazards and risks associated with its handling and use.

Check Digit Verification of cas no

The CAS Registry Mumber 1198-67-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1198-67:
(6*1)+(5*1)+(4*9)+(3*8)+(2*6)+(1*7)=90
90 % 10 = 0
So 1198-67-0 is a valid CAS Registry Number.

1198-67-0SDS

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 methyl 3,4,5-tribromo-1H-pyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 3,4,5-tribromo-pyrrole-2-carboxylic acid methyl ester

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:1198-67-0 SDS

1198-67-0Relevant articles and documents

Gatekeeping Ketosynthases Dictate Initiation of Assembly Line Biosynthesis of Pyrrolic Polyketides

Yi, Dongqi,Acharya, Atanu,Gumbart, James C.,Gutekunst, Will R.,Agarwal, Vinayak

, p. 7617 - 7622 (2021)

Assembly line biosynthesis of polyketide natural products involves checkpoints where identities of thiotemplated intermediates are verified before polyketide extension reactions are allowed to proceed. Determining what these checkpoints are and how they operate is critical for reprogramming polyketide assembly lines. Here we demonstrate that ketosynthase (KS) domains can perform this gatekeeping role. By comparing the substrate specificities for polyketide synthases that extend pyrrolyl and halogenated pyrrolyl substrates, we find that KS domains that need to differentiate between these two substrates exercise high selectivity. We additionally find that amino acid residues in the KS active site facilitate this selectivity and that these residues are amenable to rational engineering. On the other hand, KS domains that do not need to make selectivity decisions in their native physiological context are substrate-promiscuous. We also provide evidence that delivery of substrates to polyketide synthases by non-native carrier proteins is accompanied by reduced biosynthetic efficiency.

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