CYCLOHEXYLMETHYLMAGNESIUM BROMIDE

CAS No.：35166-78-0

Important Notice

This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Basic information

Product Name:	CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
Synonyms:	Cyclohexylmethylmagnesium bromide, 0.5 M in THF;Cyclohexylmethylmagnesium bromide, 0.25M solution in THF, AcroSeal;Bromo(cyclohexylmethyl)magnesium;(CyclohexylMethyl)MagnesiuM broMide, 0.5 M solution in THF, SpcSeal;Magnesium,bromo(cyclohexylmethyl)-;(cyclohexylmethyl) magnesium bromide tetrahydrofuran 0.5M;magnesium,methanidylcyclohexane,bromide;CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
CAS:	35166-78-0
MF:	C7H13BrMg
MW:	201.39
EINECS:
Product Categories:	Grignard Reagents;Organometallic Reagents;Alkyl;Chemical Synthesis;Grignard Reagents;Organometallic Reagents
Mol File:	35166-78-0.mol

CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Chemical Properties

density	0.966 g/mL at 25 °C
Fp	-17 °C
form	Solution
color	Colorless to yellow to brown

Safety Information

Hazard Codes	F,C
Risk Statements	11-14-19-34-37-40
Safety Statements	16-26-36/37/39-45
RIDADR	UN 2924 3/PG 2
WGK Germany	3
HS Code	29319090

MSDS Information

CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Usage And Synthesis

Chemical Properties	Colorless to yellow to brown liquid
Uses	Reactant involved in: Isomerization polymerization of alkenylcyclohexanes Intramolecular rearrangements of vinylidenecyclopropanes Cycloisomerization of cyclic and acyclic enynes Additionally reactant involved in synthesis of biologically active molecules including: Dipeptidyl boronic acid proteasome inhibitors Substituted 1,3-dihydroindole-2-ones with antitumor effects Sulfur-free transition state nucleoside analog inhibitors of methylthioadenosine nucleosidase and phosphorylase
Uses	Reactant involved in:• ;Isomerization polymerization of alkenylcyclohexanes1• ;Intramolecular rearrangements of vinylidenecyclopropanes2• ;Cycloisomerization of cyclic and acyclic enynes3Additionally reactant involved in synthesis of biologically active molecules including:• ;Dipeptidyl boronic acid proteasome inhibitors4• ;Substituted 1,3-dihydroindole-2-ones with antitumor effects5• ;Sulfur-free transition state nucleoside analog inhibitors of methylthioadenosine nucleosidase and phosphorylase6

CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Preparation Products And Raw materials

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