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1-Boc-4-bromo-3-hydroxymethylindole, also known as tert-butyl 1-(bromomethyl)-4-bromo-1H-indole-3-carboxylate, is a chemical compound that plays a significant role in medicinal chemistry and organic synthesis. It is a type of bromoindole and is instrumental in the production of various pharmacological agents. With a molecular formula of C14H15BrNO3 and a molar mass of 334.18 g/mol, 1-Boc-4-bromo-3-hydroxymethylindole is typically stored in a cool and dry place to maintain its stability. Due to its potential hazardous effects on the environment or human health, it requires careful handling and should be used by trained personnel.

914349-05-6

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    Cas No: 914349-05-6

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914349-05-6 Usage

Uses

Used in Medicinal Chemistry:
1-Boc-4-bromo-3-hydroxymethylindole is used as a building block in drug discovery and development for its ability to contribute to the synthesis of various pharmacological agents. Its unique structure allows for the creation of new compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 1-Boc-4-bromo-3-hydroxymethylindole is utilized as a key intermediate for the production of complex organic molecules. Its presence in the synthesis process can lead to the development of novel compounds with specific properties and functions.
Used in Pharmaceutical Industry:
1-Boc-4-bromo-3-hydroxymethylindole is used as a precursor in the synthesis of pharmaceutical agents, particularly those with potential applications in treating various diseases and conditions. Its versatility in chemical reactions makes it a valuable component in the development of new drugs.
Used in Research and Development:
In research and development settings, 1-Boc-4-bromo-3-hydroxymethylindole is employed as a tool for studying the properties and behavior of bromoindole compounds. Its use in experiments can provide valuable insights into the mechanisms of chemical reactions and the potential applications of related compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 914349-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,3,4 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 914349-05:
(8*9)+(7*1)+(6*4)+(5*3)+(4*4)+(3*9)+(2*0)+(1*5)=166
166 % 10 = 6
So 914349-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H16BrNO3/c1-14(2,3)19-13(18)16-7-9(8-17)12-10(15)5-4-6-11(12)16/h4-7,17H,8H2,1-3H3

914349-05-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-bromo-3-(hydroxymethyl)indole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Boc-4-Bromo-3-hydroxymethylindole

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:914349-05-6 SDS

914349-05-6Downstream Products

914349-05-6Relevant articles and documents

Asymmetric Total Synthesis of Sarpagine and Koumine Alkaloids

He, Ling,Jiang, Yan,Qiao, Zhen,Qiu, Hanyue,Su, Xiaojiao,Tan, Qiuyuan,Yang, Jiaojiao,Yang, Zhao,Zhang, Min,Zhou, Wenqiang

supporting information, p. 13105 - 13111 (2021/05/10)

We report here a concise, collective, and asymmetric total synthesis of sarpagine alkaloids and biogenetically related koumine alkaloids, which structurally feature a rigid cage scaffold, with L-tryptophan as the starting material. Two key bridged skeleton-forming reactions, namely tandem sequential oxidative cyclopropanol ring-opening cyclization and ketone α-allenylation, ensure concurrent assembly of the caged sarpagine scaffold and installation of requisite derivative handles. With a common caged intermediate as the branch point, by taking advantage of ketone and allene groups therein, total synthesis of five sarpagine alkaloids (affinisine, normacusine B, trinervine, Na-methyl-16-epipericyclivine, and vellosimine) with various substituents and three koumine alkaloids (koumine, koumimine, and N-demethylkoumine) with more complex cage scaffolds has been accomplished.

ANTIBACTERIAL COMPOUNDS

-

Page/Page column 36; 37, (2018/10/19)

Novel compounds having antimicrobial activitiy, in particular against Pseudomonas aeruginosa, Burkholderia cepaciaand/or Clostridium difficile, and a pharmaceutical composition containing the novel compound.

A Modular Formal Total Synthesis of (±)-Cycloclavine

Netz, Natalie,Opatz, Till

, p. 1723 - 1730 (2016/03/01)

Cycloclavine is a clavine-type Ergot alkaloid noteworthy for its unique pentacyclic skeleton featuring a 3-azabicyclo[3.1.0]hexane substructure. A short convergent route to the racemic alkaloid is described which comprises only eight linear steps and requires only four chromatographic purifications. The two key building blocks can be prepared in high yield from commercially available starting materials. Two consecutive coupling reactions, namely a selective alkylation of a dienolate and a Heck reaction, are the key steps of the reaction sequence. (Chemical Equation Presented).

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