ChemicalBook--->CAS DataBase List--->1129-28-8

1129-28-8

1129-28-8 Structure

1129-28-8 Structure
IdentificationMore
[Name]

Methyl 3-(bromomethyl)benzoate
[CAS]

1129-28-8
[Synonyms]

3-(BROMOMETHYL)BENZOIC ACID METHYL ESTER
3-CARBOMETHOXYBENZYL BROMIDE
ALPHA-BROMO-M-TOLUIC ACID METHYL ESTER
M-CARBOMETHOXYBENZYL BROMIDE
METHYL 3-(BROMOMETHYL)BENZOATE
METHYL ALPHA-BROMO-M-TOLUATE
TIMTEC-BB SBB005793
Methyl 3-(bromomethyl)benzoat
3-(BROMOMETHYL)PHENYLACETICACID
Methyl 3-(bromomethyl)benzoate ,97%
[EINECS(EC#)]

419-100-4
[Molecular Formula]

C9H9BrO2
[MDL Number]

MFCD00051437
[Molecular Weight]

229.07
[MOL File]

1129-28-8.mol
Chemical PropertiesBack Directory
[Appearance]

white crystalline powder or crystals
[Melting point ]

46-47 °C(lit.)
[Boiling point ]

112-114 °C3 mm Hg(lit.)
[density ]

1,47 g/cm3
[Fp ]

115°C/0.8mm
[storage temp. ]

2-8°C
[form ]

Crystals or Crystalline Powder
[color ]

White
[Water Solubility ]

Slightly soluble in water.
[Detection Methods]

HPLC
[BRN ]

638569
[InChI]

InChI=1S/C9H9BrO2/c1-12-9(11)8-4-2-3-7(5-8)6-10/h2-5H,6H2,1H3
[InChIKey]

YUHSMQQNPRLEEJ-UHFFFAOYSA-N
[SMILES]

C(OC)(=O)C1=CC=CC(CBr)=C1
[CAS DataBase Reference]

1129-28-8(CAS DataBase Reference)
[NIST Chemistry Reference]

Methyl 3-bromomethylbenzoate(1129-28-8)
[Storage Precautions]

Light sensitive;Store under nitrogen;Heat sensitive
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H314-H317
[Precautionary statements ]

P260-P270-P280-P301+P312-P303+P361+P353-P305+P351+P338
[Hazard Codes ]

C,Xi
[Risk Statements ]

R22:Harmful if swallowed.
R34:Causes burns.
R43:May cause sensitization by skin contact.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 3261 8/PG 2
[WGK Germany ]

2
[F ]

19
[Hazard Note ]

Irritant/Corrosive
[REACH Registrations]

Inactive
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29163990
[Storage Class]

8A - Combustible corrosive hazardous materials
[Hazard Classifications]

Acute Tox. 4 Oral
Skin Corr. 1B
Skin Sens. 1
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Petroleum ether-->Carbon tetrachloride-->N-Bromosuccinimide-->Benzoyl peroxide-->Methyl 3-methylbenzoate-->3-Hydroxymethyl-benzoic acid methyl ester-->Methanol-->3-(broMoMethyl)benzoyl chloride-->3-(Bromomethyl)benzoic acid-->AIBN
[Preparation Products]

3-((1-(tert-Butoxycarbonyl)piperidin-4-yl)methyl)benzoic acid-->Methyl 3-(aminomethyl)benzoate hydrochloride-->Methyl 3-((piperidin-4-yl)methyl)benzoate-->Di-tert-butyl hydrazodicarboxylate-->Methyl 3-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]benzoate-->Methyl 3-[4-(tert-butoxycarbonylamino)piperidin-1-yl]methylbenzoate-->Methyl 3-[(3-Formylphenoxy)methyl]benzoate-->Methyl 3-(1H-1,2,4-triazol-1-ylmethyl)benzoate-->methyl 3-((diethoxyphosphoryl)methyl)benzoate
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Methyl 3-(bromomethyl)benzoate(1129-28-8).msds
Hazard InformationBack Directory
[Chemical Properties]

white crystalline powder or crystals
[Uses]

Methyl 3-(bromomethyl)benzoate is used in organic synthesis of other chemicals.
[Synthesis]

Methyl 3-methylbenzoate

99-36-5

Methyl 3-(bromomethyl)benzoate

1129-28-8

General procedure for the synthesis of methyl 3-bromomethylbenzoate from methyl m-methylbenzoate: 30 mL of carbon tetrachloride (CCl4) and 7.9 g of methyl m-methylbenzoate were added to a dry 100 mL three-necked flask, and after dissolution, 0.23 g of AIBN (azobisisobutyronitrile) and 9.36 g of NBS (N-bromosuccinimide) were sequentially added in three additions (with an interval of about 2-3 hours). The reaction system was heated to 70°C and the color of the reaction solution was observed to change gradually from yellow to orange and finally to white. The reaction was monitored by TLC (eluent: cyclohexane/ethyl acetate = 5:1) until the reaction was almost complete. At the end of the reaction, the resulting succinimide and unreacted N-bromosuccinimide were removed by filtration. The filtrate was rotary evaporated to give 11.5 g of a yellow oily product, methyl 3-bromomethylbenzoate, in 95% yield.

[References]

[1] Organic and Biomolecular Chemistry, 2003, vol. 1, # 14, p. 2506 - 2511
[2] Patent: CN106146413, 2016, A. Location in patent: Paragraph 0027; 0028
[3] European Journal of Medicinal Chemistry, 2009, vol. 44, # 1, p. 7 - 17
[4] Molecules, 2016, vol. 21, # 12,
[5] Patent: WO2018/169777, 2018, A1. Location in patent: Paragraph 0227
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 3-(bromomethyl)benzoate(1129-28-8)MS
Methyl 3-(bromomethyl)benzoate(1129-28-8)1HNMR
Methyl 3-(bromomethyl)benzoate(1129-28-8)IR1
Methyl 3-(bromomethyl)benzoate(1129-28-8)IR2
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Methyl 3-(bromomethyl)benzoate, 95%(1129-28-8)
[Alfa Aesar]

Methyl 3-(bromomethyl)benzoate, 97%(1129-28-8)
[Sigma Aldrich]

1129-28-8(sigmaaldrich)
[TCI AMERICA]

Methyl 3-(Bromomethyl)benzoate,>97.0%(GC)(1129-28-8)
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