4-Bromoindole

Modify Date: 2024-01-02 14:24:30

4-Bromoindole Structure
4-Bromoindole structure
Common Name 4-Bromoindole
CAS Number 52488-36-5 Molecular Weight 196.044
Density 1.7±0.1 g/cm3 Boiling Point 316.9±15.0 °C at 760 mmHg
Molecular Formula C8H6BrN Melting Point 17 °C
MSDS Chinese USA Flash Point 145.5±20.4 °C
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name 4-bromo-1H-indole
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.7±0.1 g/cm3
Boiling Point 316.9±15.0 °C at 760 mmHg
Melting Point 17 °C
Molecular Formula C8H6BrN
Molecular Weight 196.044
Flash Point 145.5±20.4 °C
Exact Mass 194.968353
PSA 15.79000
LogP 2.91
Vapour Pressure 0.0±0.7 mmHg at 25°C
Index of Refraction 1.712
Storage condition 0-6°C

 Safety Information

Symbol GHS07
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:Irritant
Risk Phrases R36/37/38
Safety Phrases S26-S36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933990090

 Synthetic Route

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles4

More Articles
A concise and scalable strategy for the total synthesis of dictyodendrin B based on sequential C-H functionalization.

Angew. Chem. Int. Ed. Engl. 54(18) , 5451-5, (2015)

A sequential CH functionalization strategy for the synthesis of the marine alkaloid dictyodendrin B is reported. Our synthesis begins from commercially available 4-bromoindole and involves six direct...

Applications of vinylogous Mannich reactions. Total syntheses of the Ergot alkaloids rugulovasines A and B and setoclavine.

J. Am. Chem. Soc. 123(25) , 5918-24, (2001)

Concise syntheses of the Ergot alkaloids rugulovasine A (3a), rugulovasine B (3b), and setoclavine (2) have been completed by strategies that feature inter- and intramolecular vinylogous Mannich react...

Optically active total synthesis of clavicipitic acid. Yokoyama Y, et al.

J. Org. Chem. 60(6) , 1486-1487, (1995)

 Synonyms

5-Br-indole
4-bromo-indole
5-Bromo-1H-indole
5-bromo-indole
4-bromindole
MFCD00671502
5-BI
1H-INDOLE,4-BROMO
4-Bromo-1H-indole
5-broMo-2H-indole
1H-Indole, 4-bromo-
1H-Indole, 5-bromo-
5-bromonindole
5-Bromide indole
5-indolyl bromide
4-Brom-indol
5-Bromindole
4-Bromoindole
5-Bromoindole
Bromoindole
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