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benzyl 2-acetamido-4,6-di-O-acetyl-2-deoxy-3-O-<(R)-1-(methoxycarbonyl)ethyl>-α-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81629-37-0

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81629-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81629-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,2 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81629-37:
(7*8)+(6*1)+(5*6)+(4*2)+(3*9)+(2*3)+(1*7)=140
140 % 10 = 0
So 81629-37-0 is a valid CAS Registry Number.

81629-37-0Downstream Products

81629-37-0Relevant academic research and scientific papers

The synthesis and biological activities of anomeric butyl glycosides of muramyl dipeptide

Pertel,Kadun,Kakayan,Chirva,Krivorutchenko,Krivoshein,Bakova,Andronovskaya

, p. 628 - 634 (2007/10/03)

The synthesis of anomeric butyl glycosides of muramyl dipeptide was reported. α-Butyl glycoside of N-acetyl-D-glucosamine was 3-O-benzylidenated and the benzylidene derivative was 3-O-alkylated by the Williamson reaction with sodium (S)-2-chloropropionate

METHANOLYSIS AND AMINOLYSIS OF N-ACETYLMURAMIC ACID LACTONES: EVIDENCE FOR THE RETENTION OF THE D-gluco CONFIGURATION

Keglevic, Dina,Pongracic, Mario

, p. 85 - 100 (2007/10/02)

Methanolysis of benzyl α-glycosides of N-acetylmuramic acid lactones with HO-6 free (2) and substituted (4, 7, 10, and 12) is catalysed by small amounts of silica gel to give, exclusively, the corresponding methyl esters with HO-4 unsubstituted (3, 5, 8,

Synthesis of carbohydrate analogs (positional, configurational, and optical) of n-acetylmuramoyl-L-alanyl-D-isoglutamine, and their immunoadjuvant activities.

Hasegawa,Kaneda,Goh,Nishibori,Kiso,Azuma

, p. 143 - 163 (2007/10/02)

2-Acetamido-2-deoxy-4- and -6-O-(D-2-propanoyl-L-alanyl-D-isoglutamine)-D-glucopyranose, 2-acetamido-2-deoxy-3-O-(D-2-propanoyl-L-alanyl-D-isoglutamine)-D-allopyranose, -D-gulopyranose, -D-galactopyranose, -D-mannopyranose, and -L-idopyranose, and 3-O-(D-2-propanoyl-L-alanyl-D-isoglutamine)-D- and -L-glucopyranose were synthesized, in order to clarify the structural requirements for the immunoadjuvant activity of the carbohydrate moiety in N-acetylmuramoyl-L-alanyl-D-isoglutamine. Immunoadjuvant activity of the N-acetylmuramoyl-dipeptide analogs was examined in guinea-pigs.

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