structure of 5-Bromo-6-chloro-1H-indol-3-yl beta-D-glucopyranoside CAS 93863-89-9Custom Synthesis of Carbohydrates Iden­ti­fi­ca­tion Prop­er­ties Safe­ty Data Spec­i­fi­ca­tions and Oth­er Information Links

Iden­ti­fi­ca­tion

CAS Number

93863-89-9

Name

5-Bro­­mo-6-chloro-1H-indol-3-yl beta-D-glu­­copy­­ra­no­side

Syn­onyms

5-Brom-6-chlor-1H-indol-3-yl-β-D-glu­­copy­­ra­nosid [Ger­man] [ACD/IUPAC Name] 5-Bro­­mo-6-chloro-1H-indol-3-yl β-D-glu­­copy­­ra­no­side [ACD/IUPAC Name] β-D-Glu­­copy­­ra­no­side de 5-bro­­mo-6-chloro-1H-indol-3-yle [French] [ACD/IUPAC Name] β-D-Glu­­copy­­ra­no­side, 5-bro­­mo-6-chloro-1H-indol-3-yl [ACD/​Index Name] 5-Bro­­mo-6-chloro-3-indolyl ¦Â-D-glu­­copy­­ra­no­side 5-Bro­­mo-6-chloro-3-indolyl β-D-glu­­copy­­ra­no­side 5-Bro­­mo-6-chloro-3-indolyl-b-D-glu­­copy­­ra­no­side 5-Bro­­mo-6-chloro-3-indolyl-β-D-glu­­copy­­ra­no­side 5-BRO­­MO-6-CHLORO-3-INDOXYL-β-D-GLU­­COPY­­RA­NO­SIDE 93863-89-9 [RN] Magen­­ta-glu­­co­­side SS-7951

Mol­e­c­u­lar Structure

structure of 5-Bromo-6-chloro-1H-indol-3-yl beta-D-glucopyranoside CAS 93863-89-9

struc­ture of 5-Bro­­mo-6-chloro-1H-indol-3-yl beta-D-glu­­copy­­ra­no­side CAS 93863-89-9

SMILES

C1=C2C(=CC(=C1Br)Cl)NC=C2O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O

Std­InChI

InChI=1S/C14H15BrClNO6/c15-6-1-5-8(2-7(6)16)17-3-9(5)22-14-13(21)12(20)11(19)10(4-18)23-14/h1-3,10-14,17-21H,4H2/t10-,11-,12+,13-,14-/m1/s1

Std­InChIKey

CHRVKCMQIZYL­NM-RKQHYHRC­SA-N

Mol­e­c­u­lar Formula

C14H15BrClNO6

Mol­e­c­u­lar Weight

408.63

Prop­er­ties

Appear­ance

Off-white to white pow­der

Safe­ty Data

Per­son­al Pro­tec­tive Equipment

Eye­shields, Gloves, type N95 (US), type P1 (EN143) res­pi­ra­tor fil­ter

WGK Germany

3 

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 5-Bro­­mo-6-chloro-1H-indol-3-yl beta-D-glu­­copy­­ra­no­side CAS 93863-89-9

Stan­dard

Enter­prise stan­dard

Iden­ti­fi­ca­tion Methods

HPLC/HNMR/IR

Puri­ty

98% min

Man­u­fac­tur­ing Capacity

Per request

Stor­age

2-8 degrees Cel­sius away from light

Appli­ca­tion

Used as a phar­ma­ceu­ti­cal Inter­me­di­ate to reduce tox­i­c­i­ty ; Or as an enzyme sub­strate in Diag­nos­tic Reagents

Links

This prod­uct is devel­oped by our RandD com­pa­ny Ulcho Bio­chem­i­cal Ltd(http://​www​.ulcho​.com/), and here is the cor­re­spond­ing linkhttp://​ulcho​.com/​5​-​b​r​o​m​o​-​6​-​c​h​l​o​r​o​-​1​h​-​i​n​d​o​l​-​3​-​y​l​-​b​e​t​a​-​d​-​g​l​u​c​o​p​y​r​a​n​o​s​i​d​e​-​c​a​s​-​9​3​8​6​3​-​8​9​-9/

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