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3-acetamido-2,3,6-trideoxy-arabino-α-D,L-hexose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129172-06-1

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129172-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129172-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,7 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129172-06:
(8*1)+(7*2)+(6*9)+(5*1)+(4*7)+(3*2)+(2*0)+(1*6)=121
121 % 10 = 1
So 129172-06-1 is a valid CAS Registry Number.

129172-06-1Relevant academic research and scientific papers

DIASTEREOSELECTIVE SYNTHESIS OF N-ACETYL-D,L-ACOSAMINE AND N-BENZOYL-D,L-RISTOSAMINE

Hirama, Masahiro,Shigemoto, Takeo,Yamazaki, Yutaka,Ito, Sho

, p. 4133 - 4136 (1985)

N-Acyl derivatives of D,L-acosamine and D,L-ristosamine were synthesized with high stereoselectivity utilizing intramolecular Michael addition of γ- and δ-carbamoyloxy-α,β-unsaturated esters.

Syntheses of spacer-linked neodisaccharides derived from L-Daunosamine

Kirschning, Andreas,Chen, Guang-Wu

, p. 4665 - 4668 (2007/10/03)

The preparation of novel head-to-head spacer-linked bisdaunosamine homodimers 8, 15 and 18 is described. The synthesis is achieved by double glycosylation of monosilylated 1,4-butanediol 9 using silyl glycoside 5 as glycosyl donor. Alternatively, olefin metathesis of allyl glycosides α-11 and particularly of α-12 constitutes a second route toward 8 and its unsaturated derivative 15 while non symmetrical dimer 18 has been obtained by cross metathesis of allyl glycosides 11 and 12.

Tartraldehydes I. Synthesis of N-acetyl-D- And L-daunosamine and their xylo isomers

Herczegh, Pal,Zsely, Martina,Kovacs, Imre,Batta, Gyula,Sztaricskai, Ferenc J.

, p. 1195 - 1198 (2007/10/02)

The title compounds were prepared from tartraldehyde dithioacetals 1 and 3 using Wittig chain elongation, amino functionalization of the double bond and removal of the protective groups.

THE SYNTHESIS OF 3-ACETAMIDO-2,3,5,6-TETRADEOXY-5-FLUORO-D,L-ribo-HEXOFURANOSE BY THE DIRECT FLUORINATION OF METHYL 3-ACETAMIDO-2,3,6-TRIDEOXY-D,L-arabino-HEXOPYRANOSIDE (METHYL N-ACETYL-D,L-ACOSAMINIDE)

Welch, John T.,Svahn, Britt-Marie,Eswarakrishnan, Seetha,Hutchinson, John P.,Zubieta, Jon

, p. 221 - 232 (2007/10/02)

3-Acetamido-2,3,5,6-tetradeoxy-5-fluoro-D,L-ribo-hexofuranose was synthesized by direct, fluorinative dehydroxylation of methyl 3-acetamido-2,3,6-trideoxy-D,L-arabino-hexopyranoside with sulfur tetrafluoride-hydrogen fluoride.The furanose form and the ribo configuration, indicated by 13C- and 1H-n. m. r. spectroscopy, respectively, were confirmed by a single-crystal, X-ray diffraction study.

STEREOSELECTIVE SYNTHESIS OF L-DAUNOSAMINE

Mukaiyama, Teruaki,Goto, Yukihisa,Shoda, Shin-ichiro

, p. 671 - 674 (2007/10/02)

L-Daunosamine was conveniently synthesized from β-amino amide 1 obtained by stereoselective addition of α-lithio N,N-dimethylacetamide to the imine of 2,3-O-cyclohexylidene-4-deoxy-L-threose in the presence of zinc halide.

Convenient Synthesis of L-Digitoxose, L-Cymarose and L-Ristosamine

Brimacombe, John S.,Hanna, Roderick,Saeed, May S.,Tucker, Leslie C. N.

, p. 2583 - 2588 (2007/10/02)

Methyl 2,3-O-benzylidene-6-deoxy-4-O-(2-methoxyethoxymethyl)-α-L-mannopyranoside (10) and the 4-O-(methoxymethyl) analogue (11) reacted with butyl-lithium to give the 4-O-substituted methyl 2,6-dideoxy-α-L-erythro-hexopyranosid-3-uloses (12) and (13), res

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