CAS 1521-51-3|3-Bromocyclohexene

Introduction：Basic information about CAS 1521-51-3|3-Bromocyclohexene, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Chemical & Physical Properties
3. Safety Information
4. Customs
5. Articles2
6. Synonyms

Common Name	3-Bromocyclohexene
CAS Number	1521-51-3	Molecular Weight	161.04000
Density	1.4 g/mL at 25 °C(lit.)	Boiling Point	57-58 °C12 mm Hg(lit.)
Molecular Formula	C₆H₉Br	Melting Point	/
MSDS	ChineseUSA	Flash Point	130 °F
Symbol	GHS02, GHS07	Signal Word	Warning

Names

Name	3-Bromocyclohexene
Synonym	More Synonyms

Chemical & Physical Properties

Density	1.4 g/mL at 25 °C(lit.)
Boiling Point	57-58 °C12 mm Hg(lit.)
Molecular Formula	C₆H₉Br
Molecular Weight	161.04000
Flash Point	130 °F
Exact Mass	159.98900
LogP	2.49000
Vapour Pressure	5.49mmHg at 25°C
Index of Refraction	n20/D 1.528(lit.)
InChIKey	AJKDUJRRWLQXHM-UHFFFAOYSA-N
SMILES	BrC1C=CCCC1
Storage condition	2-8°C

Safety Information

Symbol	GHS02, GHS07
Signal Word	Warning
Hazard Statements	H226-H315-H319-H335
Precautionary Statements	P261-P305 + P351 + P338
Personal Protective Equipment	Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes	Xi
Risk Phrases	R10
Safety Phrases	S26-S36
RIDADR	UN 1993 3/PG 3
WGK Germany	3
Packaging Group	III
HS Code	2903890090

Customs

HS Code	2903890090
Summary	2903890090. halogenated derivatives of cyclanic, cyclenic or cyclotherpenic hydrocarbons. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles2

An efficient synthesis of N-tert-butoxycarbonyl-O-cyclohexyl-L-tyrosine.

Chem. Pharm. Bull. 49(2) , 233-5, (2001)

A facile and efficient synthesis of N-tert-butoxycarbonyl-O-cyclohexyl-L-tyrosine [Boc-Tyr(Chx)-OH] is described. Boc-Tyr-OH was treated with NaH in dimethylformamide and then with 3-bromocyclohexene ...

Synthesis of enantiopure cyclitols from (±)-3-bromocyclohexene mediated by intramolecular oxyselenenylation employing (S, S)-hydrobenzoin and (S)-mandelic acid as chiral sources. Lee YJ, et al.

Tetrahedron 61(8) , 1987-2001, (2005)

Synonyms

3-Bromocyclohex-1-ene

1,2,3,4-Tetrahydrobromobenzene

MFCD00013775

3-BroMocyclohexene

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