(S)-(1-Chloroethyl)benzene

95%

Reagent Code: #233358
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CAS Number 3756-41-0

science Other reagents with same CAS 3756-41-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 140.61 g/mol
Formula C₈H₉Cl
badge Registry Numbers
MDL Number MFCD20621165
thermostat Physical Properties
Boiling Point 80.5-82.5 °C at 17 mmHg
inventory_2 Storage & Handling
Density 1.046±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

(S)-(1-Chloroethyl)benzene is a chiral alkylating agent and synthetic intermediate in organic chemistry. It is primarily used to introduce the (S)-1-phenylethyl group into molecules during alkylation reactions, enabling the synthesis of enantiomerically pure compounds. This makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where stereochemical control is crucial. The compound facilitates stereoselective transformations in multi-step syntheses, particularly for active pharmaceutical ingredients requiring specific chirality. It is also applied in the preparation of optically active materials and as a reagent in coupling reactions for complex molecular architectures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,360.00
inventory 250mg
10-20 days ฿12,180.00
inventory 1g
10-20 days ฿36,880.00
(S)-(1-Chloroethyl)benzene
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(S)-(1-Chloroethyl)benzene is a chiral alkylating agent and synthetic intermediate in organic chemistry. It is primarily used to introduce the (S)-1-phenylethyl group into molecules during alkylation reactions, enabling the synthesis of enantiomerically pure compounds. This makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where stereochemical control is crucial. The compound facilitates stereoselective transformations in multi-step syntheses, particularly for acti

(S)-(1-Chloroethyl)benzene is a chiral alkylating agent and synthetic intermediate in organic chemistry. It is primarily used to introduce the (S)-1-phenylethyl group into molecules during alkylation reactions, enabling the synthesis of enantiomerically pure compounds. This makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where stereochemical control is crucial. The compound facilitates stereoselective transformations in multi-step syntheses, particularly for active pharmaceutical ingredients requiring specific chirality. It is also applied in the preparation of optically active materials and as a reagent in coupling reactions for complex molecular architectures.

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