3-Bromo-5-iodobenzoic acid

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Names

[ Name ]:
3-Bromo-5-iodobenzoic acid

[Synonym ]:
3-Bromo-5-iodobenzoic acid
5-iodo-3-bromo-benzoic acid
3-Brom-5-jod-benzoesaeure
5-bromo-3-iodobenzoic acid
3-bromo-5-iodo-benzoic acid
Benzoic acid, 3-bromo-5-iodo-
3-iodo-5-bromobenzoic acid
3-bromo-5-iodobenzenecarboxylic acid
MFCD00191851

Chemical & Physical Properties

[ Density]:
2.3±0.1 g/cm3

[ Boiling Point ]:
385.2±37.0 °C at 760 mmHg

[ Melting Point ]:
219-221 °C(lit.)

[ Molecular Formula ]:
C₇H₄BrIO₂

[ Molecular Weight ]:
326.914

[ Flash Point ]:
186.8±26.5 °C

[ Exact Mass ]:
325.843933

[ PSA ]:
37.30000

[ LogP ]:
3.93

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.693

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2916399090

Precursor & DownStream

Precursor

DownStream

3-Bromo-5-iodoaniline
3-Bromo-5-hydroxybenzoic acid
Methyl 3-bromo-5-iodobenzoate
2-[2-(2-methoxyethoxy)ethoxy]ethyl 3,5-diethynylbenzoate

Customs

[ HS Code ]: 2916399090

[ Summary ]:
2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Reaction of iodonium ylides of 1,3-dicarbonyl compounds with HF reagents.

Molecules 17(6) , 6625-32, (2012)

Reaction of dibenzoylmethane with (diacetoxyiodo)benzene in the presence of KOH in MeCN quantitatively gave the corresponding iodonium ylide, which was treated with a HF reagent to afford the correspo...

Comparison of three gamma-turn mimetic scaffolds incorporated into angiotensin II.

Bioorg. Med. Chem. 8(9) , 2375-83, (2000)

Rigidification of peptides by cyclization and iterative incorporation of well-defined secondary structure mimetics constitutes one approach to the design of non-peptidergic structures with better defi...

A scalable synthesis of the thromboxane receptor antagonist 3-{3-[2-(4-chlorobenzenesulfonamido) ethyl]-5-(4-fluorobenzyl) phenyl} propionic acid via a regioselective Heck cross-coupling strategy. Waite DC and Mason CP.

Org. Process Res. Dev. 2(2) , 116-20, (1998)

3-bromo-5-iodobenzoic acid ethyl ester
3-Bromo-5-chloro-2-iodobenzoic acid
3-Bromo-2-fluoro-5-iodobenzoic acid
2-Bromo-5-iodobenzoic acid
2,3,5-Iodobenzoic acid
2-[[[(5-BROMO-2-METHOXYBENZOYL)AMINO]THIOXOMETHYL]AMINO]-5-IODO-BENZOIC ACID
(E)-N-(3-ethyl-6,7-dihydro-[1,4]dioxino[2',3':4,5]benzo[1,2-d]thiazol-2(3H)-ylidene)-2-propylpentanamide
(E)-N-(3-methyl-6,7-dihydro-[1,4]dioxino[2',3':4,5]benzo[1,2-d]thiazol-2(3H)-ylidene)-2-(N-methylmethylsulfonamido)acetamide
1a(2)-Ethyl-4-methoxy[1,4a(2)-bipiperidine]-4a(2)-methanamine
(E)-N-(3-methyl-6,7-dihydro-[1,4]dioxino[2',3':4,5]benzo[1,2-d]thiazol-2(3H)-ylidene)pyrazine-2-carboxamide
(4-(4-Chlorobenzyl)morpholin-2-yl)methanol
n-(4-(Methylsulfonyl)benzyl)pyrimidin-2-amine
(Z)-methyl 2-(2-((2,3-dihydrobenzo[b][1,4]dioxine-2-carbonyl)imino)-6,7-dihydro-[1,4]dioxino[2',3':4,5]benzo[1,2-d]thiazol-3(2H)-yl)acetate
2-[[2-(4-Phenyl-1-piperazinyl)ethyl]amino]ethanol
2-[[2-[4-(Phenylmethyl)-1-piperazinyl]ethyl]amino]ethanol
4-Methyl-1-[(1-prop-2-ynylpiperidin-4-yl)methyl]piperidine

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