structure of 6-Chloro-1H-Indol-3-Yl-beta-D-Galactopyranoside CAS 138182-21-5Custom Synthesis of Carbohydrates Iden­ti­fi­ca­tion Prop­er­ties Safe­ty Data Spec­i­fi­ca­tions and Oth­er Information Links

Iden­ti­fi­ca­tion

CAS Number

138182-21-5

Name

6-Chloro-1H-Indol-3-Yl-beta-D-Galac­­topy­­ra­no­side

Syn­onyms

6-Chlor-1H-indol-3-yl-β-D-galac­­topy­­ra­nosid [Ger­man] [ACD/IUPAC Name] 6-Chloro-1H-indol-3-yl β-D-galac­­topy­­ra­no­side [ACD/IUPAC Name] β-D-Galac­­topy­­ra­no­side de 6-chloro-1H-indol-3-yle [French] [ACD/IUPAC Name] β-D-Galac­­topy­­ra­no­side, 6-chloro-1H-indol-3-yl [ACD/​Index Name] (2S,3R,4S,5R,6R)-2-((6-Chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (2S,3R,4S,5R,6R)-2-[(6-chloro-1H-indol-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138182-21-5 [RN] 6-chloro-1H-indol-3-yl-b-D-galac­­topy­­ra­no­side 6-Chloro-1H-indol-3-yl-β-D-galac­­topy­­ra­no­side 6-Chloro-3-indolyl ¦Â-D-galac­­topy­­ra­no­side 6-Chloro-3-indolyl β-D-galac­­topy­­ra­no­side 6-Chloro-3-indolyl-b-D-galac­­topy­­ra­no­side MFCD00467206 [MDL num­ber] MFCD01310928 [MDL num­ber] Rose-Gal Salmon-Gal

Mol­e­c­u­lar Structure

structure of 6-Chloro-1H-Indol-3-Yl-beta-D-Galactopyranoside CAS 138182-21-5

struc­ture of 6-Chloro-1H-Indol-3-Yl-beta-D-Galac­­topy­­ra­no­side CAS 138182-21-5

SMILES

C1=CC2=C(C=C1Cl)NC=C2O[C@H]3[C@@H]([C@H]([C@H]([C@H](O3)CO)O)O)O

Std­InChI

InChI=1S/C14H16ClNO6/c15-6-1-2-7-8(3-6)16-4-9(7)21-14-13(20)12(19)11(18)10(5-17)22-14/h1-4,10-14,16-20H,5H2/t10-,11+,12+,13-,14-/m1/s1

Std­InChIKey

OQW­BAXB­VBGN­SPW-MBJX­­GIAVSA-N

Mol­e­c­u­lar Formula

C14H16ClNO6

Mol­e­c­u­lar Weight

329.73

Prop­er­ties

Appear­ance

Off-white to white pow­der

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 6-Chloro-1H-Indol-3-Yl-beta-D-Galac­­topy­­ra­no­side CAS 138182-21-5

Stan­dard

Enter­prise stan­dard

Iden­ti­fi­ca­tion Methods

HPLC/HNMR/IR

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/​6​-​c​h​l​o​r​o​-​1​h​-​i​n​d​o​l​-​3​-​y​l​-​b​e​t​a​-​d​-​g​a​l​a​c​t​o​p​y​r​a​n​o​s​i​d​e​-​c​a​s​-​1​3​8​1​8​2​-​2​1​-5/

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