Lot numbers can be found on the outside label of a product:
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Structure of 1985-12-2
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4-Bromophenylisothiocyanate features a brominated aromatic ring paired with a reactive isothiocyanate group, enabling efficient conjugation in bioconjugation and materials chemistry. This bench-stable reagent facilitates site-specific labeling and functionalization under standard conditions.
4-Bromophenylisothiocyanate serves as a versatile building block for constructing thiourea and thiadiazole derivatives in medicinal chemistry and materials science. Its bromine substituent enables subsequent cross-coupling reactions, while the isothiocyanate group facilitates rapid conjugation with amines under mild conditions. The compound exhibits good bench stability and ease of purification, making it suitable for multi-step synthesis and API development workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS08
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Signal Word : Danger
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UN#: 2923
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Class : 8 (6.1)
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Packing Group : Ⅱ
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Hazard Statements : H302-H312-H314-H332-H334-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P285-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: