3-Bromo-2-methyl-1-propene

HCID 357785

Basic information

CAS
1458-98-6
Standard SMILES
C=C(C)CBr
InChIKey
USEGQJLHQSTGHW-UHFFFAOYSA-N
Molecular formula
C4H7Br
Average molar mass
135 g/mol
Monoisotopic mass
133.97311232

Names & identifiers

Preferred name
3-Bromo-2-methyl-1-propene
IUPAC
3-bromo-2-methylprop-1-ene
English name
3-Bromo-2-methylpropene
Molecular formula
C4H7Br
Molecular weight
135

Names & synonyms

3-Bromo-2-methyl-1-propeneMethallyl bromideRefChem:498491604-496-53-Bromo-2-methylpropene1458-98-63-bromo-2-methylprop-1-ene2-(Bromomethyl)prop-1-ene2-Methylallyl Bromide1-Propene, 3-bromo-2-methyl- (9CI)MFCD001341553-bromo-2-methyl-prop-1-ene
Show more names
2-methylallylbromide3-Bromo-2-methyL2-(bromomethyl)propene33-bromo-2-methylpropene
1-Propene, 3-bromo-2-methyl-Methylallyl bromide3-bromo-2-methyl propene2-Methyl-2-propenyl Bromidemethallylbromide1-Bromo-2-methyl-2-propeneNSC6173103bromo-2-methylpropene

Database identifiers

CAS
1458-98-6
PubChem CID
357785
DTXSID
DTXSID80326816
EC Number
604-496-5
Nikkaji
J461.282E

Properties

Computed structural properties

XLogP
2.3
Topological polar surface area
0 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
0
Rotatable bonds
1
Heavy atoms
5

Experimental & physicochemical properties

SpringerMaterials PropertiesSchoenflies notation

Physicochemical properties

Melting point
-115.07 °C · -115.07°C (estimate)
Boiling point
94 · 94-95 °C (lit.)
Density
1.339 g/mL · 1.339 g/mL at 25 °C (lit.)
refractive index
20 · n20/D 1.472(lit.)
Flash point
44 °F · 44 °F
storage temp.
2 · 2-8°C

Safety & regulation

GHS classification

GHS Classification · 4 items

Danger

H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P273, P280, P301+P317, P301+P330+P331, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P321, P330, P363, P370+P378, P391, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 51 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Hazard Classes and CategoriesFlam. Liq. 2 (100%)

Safety data

PPE
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
wgk
3
ridadr
UN 2924 3/PG 2
hs_code
29033990
risk_code
11-20/22-34-51/53
Signal word
Danger

Chemistry & industry

Applications · 3 items

Uses3-Bromo-2-methylpropene may be used:in the synthesis of alkenyl iminesin the synthesis of 2-methylpropenyl (“methallyl”) complex, Cp*Os(η3-allyl)Br2in a study of chiral phase transfer alkylation leading to (S)-α-alkylcysteines

Uses3-Bromo-2-methylpropene is used as a general reagent for various organic reactions and primarily for amino acid synthesis and asymmetric amino acid synthesis.

General DescriptionRotational isomerism in 3-bromo-2-methylpropene has been studied by IR spectroscopy.

Preparation methods · 1 item

Preparationmol of 4-bromotoluene was added to the reaction vessel, the temperature was raised to 65 °C, and 7 mol of 25% oxalic acid solution was added. After the addition was complete, 6 mol of methylallyl bromide was added. After the addition was complete, the mixture was refluxed for 80 min, and then distilled under reduced pressure at 15 kPa. The fraction at 55 °C was collected. The collected distillate was washed with 35% potassium bicarbonate solution, allowed to stand and separate into layers, and the oil layer was removed. The oil layer was washed with 20% potassium bromide solution, 80% triethylamine solution, and 90% propionitrile solution. The oil layer was then dehydrated with a solid phosphorus pentoxide dehydrating agent to obtain 562.55 g of the product 3-bromo-2-methylpropene, with a yield of 93%.

Suppliers100 total

常州帝通化工有限公司+86-0519-88298848 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
郑州阿尔法化工有限公司+86-18530059196 · [email protected]
衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]

Related reactions

234 records

Compound notes

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