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677914

Sigma-Aldrich

2,4-Dibromothiazole

97%

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About This Item

Empirical Formula (Hill Notation):
C3HBr2NS
CAS Number:
4175-77-3
Molecular Weight:
242.92
MDL number:
MFCD01318994
UNSPSC Code:
12352100
PubChem Substance ID:
24885405
NACRES:
NA.22

Quality Level

100

Assay

97%

form

solid

mp

80-84 °C

functional group

bromo

SMILES string

Brc1csc(Br)n1

InChI

1S/C3HBr2NS/c4-2-1-7-3(5)6-2/h1H

InChI key

MKEJZKKVVUZXIS-UHFFFAOYSA-N

Related Categories

Application

Building block in a synthesis of Melithiazole C employing a highly (E)-selective cross-metathesis between the derived 4-vinylthiazole and a dienote side-chain.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H315,H318,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

677914-1G:
677914-BULK:
677914-5G:
677914-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBK7547V
MKBG4447V
MKBF0095V
MKBC3345
MKBC1836

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Julian Gebauer et al.
Organic letters, 9(17), 3425-3427 (2007-07-20)
A short and convergent synthesis of the myxobacterial antibiotic melithiazole C is described featuring a highly E-selective cross-metathesis as the key step.

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