Name | 3-Methoxybenzyl chloride |
Synonyms | 3-Methoxybenzyl chlo m-Methoxybenzyl chloride 3-Methoxybenzyl chloride a-Chloro-m-methoxytoluene alpha-Chloro-3-methoxytoluene 1-Chloromethyl-3-methoxybenzene (3-Methoxyphenyl)methyl chloride 1-Methoxy-3-(chloromethyl)benzene 3-Methoxy-1-(chloromethyl)benzene 1-(Chloromethyl)-3-methoxybenzene, 3-(Chloromethyl)phenyl methyl ether, 3-(Chloromethyl)anisole |
CAS | 824-98-6 |
EINECS | 212-541-1 |
InChI | InChI=1/C8H9ClO/c1-10-8-4-2-3-7(5-8)6-9/h2-5H,6H2,1H3 |
InChIKey | VGISFWWEOGVMED-UHFFFAOYSA-N |
Molecular Formula | C8H9ClO |
Molar Mass | 156.61 |
Density | 1.078g/mLat 25°C(lit.) |
Melting Point | 101.67°C |
Boling Point | 124°C13mm Hg(lit.) |
Flash Point | 215°F |
Vapor Presure | 0.0284mmHg at 25°C |
Appearance | clear liquid |
Specific Gravity | 1.157 (20/4℃) |
Color | Colorless to Light yellow |
BRN | 636684 |
Storage Condition | 2-8°C |
Sensitive | Moisture Sensitive |
Refractive Index | n20/D 1.544(lit.) |
Physical and Chemical Properties | Colorless to light yellow liquid |
Use | For the synthesis of new anti-cardiovascular drugs clonidine hydrochloride and other important intermediates, but also other fine chemical raw materials |
Hazard Symbols | C - Corrosive |
Risk Codes | 34 - Causes burns |
Safety Description | 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 the label whenever possible.) |
UN IDs | UN 3265 8/PG 2 |
WGK Germany | 1 |
FLUKA BRAND F CODES | 19-21 |
HS Code | 29093090 |
Hazard Class | 8 |
Packing Group | III |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
Overview | 3-methoxybenzyl chloride is an organic halide that can be used as a pharmaceutical intermediate, it is an important intermediate for the synthesis of clonidine hydrochloride, an anti-cardiovascular drug. It can also be used for other purposes by using its chlorobenzyl property. |
production method | before, the main method for producing 3-methoxybenzyl chloride is: 3-methoxybenzaldehyde is reduced by Raney nickel to obtain 3-methoxybenzyl alcohol, and then prepared by catalytic chlorination of dichlorosulfoxide to obtain 3-methoxybenzylchloride. |
purpose | for the synthesis of important intermediates of new anti-cardiovascular drugs such as clonidine hydrochloride, it is also an important intermediate for the synthesis of new anti-cardiovascular drugs, such as clonidine hydrochloride, it is also the raw material of other fine chemicals |