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Acros Organics & Maybridge - D

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D<br />

Dibromodimet http://www.maybridge.com<br />

1,3-Dibromo-5,5-dimethylhydantoin<br />

APPLICATION GUIDE<br />

Deprotecting Group Chemistry<br />

* Deprotection of dithianes Transacetalation of dithianes to diethyl acetals using 1eq. of DBH in<br />

ethanol. S 1992, 965<br />

Fluorination<br />

* Bromofluorination of alkenes In combination with Hydrogen Fluoride-Pyridine complex or Silicon (IV)<br />

Fluoride. TL 1991, 32, 69<br />

* Bromofluorination of alkynes Reaction gives (E)-bromofluoroalkenes. Useful intermediates for Pd<br />

Coupling. TL 1991, 32, 69<br />

* Dithiolanes to gem difluoro compounds JOC 1986, 51, 3508<br />

Halogenation<br />

* Arene to haloarene Bromination of aromatic rings, even electron deficient ones, occurs in the<br />

presence of strong acids. BCJ 1994, 67, 1918<br />

* Arene to haloarene Electrophilic bromination of electron rich aromatics. TL 1997, 38, 4415<br />

* Arene to haloarene Superior to NBS for the regioselective radical bromination of pyrrole in the 2position.<br />

OSC 1998, 9, 121<br />

* Benzylic Halogenation Particularly useful for the formation of acid sensitive benzylic bromides -<br />

better than NBS for these types of compound. Radical bromination in carbon tetrachloride. JOC<br />

1987, 52, 4477<br />

Oxidation<br />

* Epoxidation Bromohydration of alkenes to form epoxides. JCS(P1) 1991, 2373<br />

1,3-Dibromo-5,5-dimethylhydantoin, 98%<br />

<strong>Acros</strong> <strong>Organics</strong> Product code Packaging Pack size Price<br />

169540250 Plastic bottle 25 g INR 810<br />

169545000 Plastic bottle 500 g INR 1,450<br />

R8 R22 R34 R50<br />

S17 S26 S36/37/39<br />

S45 S61<br />

Moisture sensitive<br />

C 5 H 6 Br 2 N 2 O 2<br />

CAS: 77-48-5<br />

MFCD00003189<br />

FW: 285.91<br />

mp: 187-191 °C (D)<br />

Fp: 155 °C<br />

1,3-Dibromo-5,5-dimethyl-2,4-imidazolidinedione , see 1,3-Dibromo-5,5-dimethylhydantoin on page<br />

706<br />

Dibromodimethylstannane , see Dimethyltin bromide on page 912<br />

4',5'-Dibromo-2',7'-dinitrofluorescein, disodium salt , see Eosin B on page 948<br />

1,2-Dibromo-1,2-diphenylethane, 96%<br />

<strong>Acros</strong> <strong>Organics</strong> Product code Packaging Pack size Price<br />

147950050 Glass bottle 5 g INR 3,010<br />

147950250 Glass bottle 25 g INR 6,510<br />

R36/37/38<br />

S24/25<br />

Lachrymator<br />

C14H12Br2 CAS: 5789-30-0<br />

MFCD00000137<br />

1,12-Dibromododecane, 96%<br />

C6H5CH(Br)CH(Br)C6H5 FW: 340.05<br />

mp: 235-241 °C (.)<br />

<strong>Acros</strong> <strong>Organics</strong> Product code Packaging Pack size Price<br />

158450050 Glass bottle 5 g INR 710<br />

158450250 Glass bottle 25 g INR 2,080<br />

158451000 Glass bottle 100 g INR 6,810<br />

158455000 Glass bottle 500 g INR 21,320<br />

S24/25 C 12 H 24 Br 2 Br(CH 2 ) 12 Br<br />

CAS: 3344-70-5<br />

MFCD00000226<br />

FW: 328.13<br />

mp: 37-42 °C<br />

O Br<br />

N<br />

N O<br />

bp: 215 °C (15 mmHg)<br />

Fp: >110 °C<br />

706 Please enquire for bulk quantities<br />

Br<br />

1,1-Dibromoethane, stabilized<br />

APPLICATION GUIDE<br />

Halogenation<br />

* C-Metal Halogenation Reacts with aryl and vinyl lithiums to produce bromides. JOC 1992, 57,<br />

2495; JOC 1985, 50, 5436<br />

Organometallic Chemistry<br />

* Grignard reaction Activates magnesium towards Grignard formation. Also activates zinc.<br />

1,1-Dibromoethane, 99%<br />

stabilized<br />

<strong>Acros</strong> <strong>Organics</strong> Product code Packaging Pack size Price<br />

406480250 Glass bottle 25 g INR 6,820<br />

406481000 Glass bottle 100 g INR 16,100<br />

R20/21/22 R40<br />

S36/37 S45<br />

C2H4Br2 CAS: 557-91-5<br />

MFCD00041719<br />

CH3CHBr2 FW: 187.86<br />

bp: 107 °C<br />

d: 2.060<br />

n 20<br />

D : 1.509 -1.512<br />

1,2-Dibromoethane<br />

APPLICATION GUIDE<br />

Alkylation<br />

* C-Alkylation Synthesis of functionalised styrenes from 1,2-DBE and arylboronic acids. OL 2003,<br />

2891<br />

* O-Alkylation Reacts with phenols to give 2-phenoxyethyl bromides. JOU 2000, 36, 254<br />

Halogenation<br />

* Arene to haloarene Reacts with aryl and vinyl lithiums to generate corresponding bromo<br />

compounds. JOC 1985, 50, 5436<br />

Organometallic Chemistry<br />

* Grignard reaction Activating agent in formation of Grignard reagents from less reactive halides by the<br />

entrainment method. S 1981, 585<br />

1,2-Dibromoethane, 99%<br />

<strong>Acros</strong> <strong>Organics</strong> Product code Packaging Pack size Price<br />

112790250 Glass bottle 25 ml INR 1,040<br />

112795000 Glass bottle 500 ml INR 2,490<br />

112790010 Glass bottle 1 l INR 3,190<br />

R45 R23/24/25 R36/<br />

37/38 R51/53<br />

S53 S45 S61<br />

Light sensitive<br />

C2H4Br2 CAS: 106-93-4<br />

MFCD00000233<br />

FW: 187.86<br />

(1,2-Dibromoethyl)benzene, 97%<br />

BrCH 2 CH 2 Br<br />

mp: 9-10 °C<br />

bp: 131-132 °C<br />

Fp: >104 °C<br />

d: 2.173<br />

n 20<br />

D : 1.5375 -1.5395<br />

<strong>Acros</strong> <strong>Organics</strong> Product code Packaging Pack size Price<br />

299300050 Glass bottle 5 g INR 1,950<br />

299305000 Plastic bottle 500 g INR 10,860<br />

R34<br />

S25 S36/37/39 S45<br />

Lachrymator<br />

C 8 H 8 Br 2<br />

CAS: 93-52-7<br />

MFCD00000138<br />

FW: 263.95<br />

mp: 68-73 °C<br />

bp: 139-141 °C (15<br />

mmHg)<br />

d: 1.740<br />

Br<br />

Br

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