3-Methylbenzyl bromide

97%

Reagent Code: #205967
label
Alias 3-methylbenzyl bromide; 3-methylbenzyl bromide; m-methylbenzyl bromide
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CAS Number 620-13-3

science Other reagents with same CAS 620-13-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.06 g/mol
Formula C₈H₉Br
badge Registry Numbers
EC Number 210-625-2
MDL Number MFCD00000177
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a benzylating agent to introduce the 3-methylbenzyl group into target molecules. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) where a substituted benzyl moiety enhances biological activity. Also utilized in the development of fragrances and functionalized materials due to its reactivity in nucleophilic substitution reactions. Its structure allows for further functionalization on the aromatic ring, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿400.00
5g
10-20 days ฿1,060.00
25g
10-20 days ฿3,490.00
100g
10-20 days ฿13,350.00
3-Methylbenzyl bromide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a benzylating agent to introduce the 3-methylbenzyl group into target molecules. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) where a substituted benzyl moiety enhances biological activity. Also utilized in the development of fragrances and functionalized materials due to its reactivity in nucleophilic substitution reactions. Its structure allo

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a benzylating agent to introduce the 3-methylbenzyl group into target molecules. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) where a substituted benzyl moiety enhances biological activity. Also utilized in the development of fragrances and functionalized materials due to its reactivity in nucleophilic substitution reactions. Its structure allows for further functionalization on the aromatic ring, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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