Cyanomethyl 2,3,4,6-Tetra-O-acetyl-1-thio-ß-D-galactopyranoside
Share product
- structure.search.product.name Cyanomethyl 2,3,4,6-Tetra-O-acetyl-1-thio-ß-D-galactopyranoside
- Product Code: TRC-C981950
- CAS Number: 61145-33-3
- Brand: TRC
Product Overview
Product Code
TRC-C981950
CAS Number
Product Format
Neat
Molecular Formula
C16 H21 N O9 S
Molecular Weight
403.40
Product Categories
Product Type
Bioactive Small MoleculeDocumentation
Looking for another lot?
To view all certificates of analysis immediately, please login to your account
or
Email download link
{{ errors.first('RequestCoaForm.lotNumber') }}
{{ errors.first('RequestCoaForm.requestEmail') }}
For information about our data processing activities, please visit our Privacy Notice.
Enter your email address and we'll email you the relevant CoA for lots:
{{ coaPopupData.packSize.coaSelectedLotNumbers }}
{{ errors.first('SendDownloadCoaLinkForm.coaEmail') }}
We will be sending the CoA to your email address {{ coaEmailPopupData.userEmail }}
Your request has been sent to our sales team to process.
Find an SDS for your region
{{ errors.first('RequestSdsForm.selectedRegion') }}
{{ errors.first('RequestSdsForm.sdsEmail') }}
For information about our data processing activities, please visit our Privacy Notice.
Your request has been sent to our sales team to process.
Product Information
Chemical Data
Analyte Name
Cyanomethyl 2,3,4,6-Tetra-O-acetyl-1-thio-beta-D-galactopyranoside
CAS Number
61145-33-3
Molecular Formula
C16 H21 N O9 S
Molecular Weight
403.40
Accurate Mass
403.0937
SMILES
CC(=O)OC[C@H]1O[C@@H](SCC#N)[C@H](OC(=O)C)[C@@H](OC(=O)C)[C@H]1OC(=O)C
InChI
InChI=1S/C16H21NO9S/c1-8(18)22-7-12-13(23-9(2)19)14(24-10(3)20)15(25-11(4)21)16(26-12)27-6-5-17/h12-16H,6-7H2,1-4H3/t12-,13+,14+,15-,16+/m1/s1
IUPAC
[(2R,3S,4S,5R,6S)-3,4,5-triacetyloxy-6-(cyanomethylsulfanyl)oxan-2-yl]methyl acetate
Product Data
Storage Temperature
-20°C
Shipping Temperature
Room Temperature
Country of Origin
CANADA
Product Format
Neat
Product Description
The nitrile of the cyanomethyl group can be converted to a methyl imidate group by treatment with sodium methoxide or HCl which can be used to attach the sugar to a protein.
References: Lee, Y-C, et al.: Biochemistry, 15, 18, 3956 (1976), Lee, Y-C, et al.: Biochemistry, 19, 4899 (1980)