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4,6-O-benzylidene-1,2-dideoxy-D-glucose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13035-13-7

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13035-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13035-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,3 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13035-13:
(7*1)+(6*3)+(5*0)+(4*3)+(3*5)+(2*1)+(1*3)=57
57 % 10 = 7
So 13035-13-7 is a valid CAS Registry Number.

13035-13-7Relevant academic research and scientific papers

GLYCOSAMINOGLYCAN (GAG) MIMETICS

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Page/Page column 19, (2010/02/12)

The invention relates to compounds that are designed to mimic the structure of GAGs; methods for the preparation of the compounds; compositions comprising the compounds; and use of the compounds and compositions thereof for the anti-angiogenic, anti-metas

Biomimetic cyclisation of prebrevetoxin polyepoxide models

Kelly, David R.,Nally, James

, p. 3251 - 3254 (2007/10/03)

(E)-1,3-Dihydroxyhex-4-ene and (E)-1,3-dihydroxy-4-methylhex-4-ene undergo epoxidation with peracetic acid and in situ cyclisation to give a mixture of tetrahydro-furans and -pyrans, whereas comparable compounds lacking the allylic hydroxyl group give pre

Die Struktur von Maitotoxin - I: Konfiguration der C1-C14-Seitenkette

Sasaki, Makoto,Matsumori, Nobuaki,Maruyama, Takahiro,Nonomura, Taro,Murata, Michio,et al.

, p. 1782 - 1785 (2007/10/03)

Keywords: Konfigurationsbestimmung; Konformation; Maitotoxin; Naturstoffe; NMR-Spektroskopie

Asymmetric Michael Addition with Amino Alcohol Catalysts Derived from D-Glucose

Wang, Feng,Tada, Masahiro

, p. 2989 - 2992 (2007/10/02)

An enantioselective Michael addition of thiophenols to 2-cyclohexen-1-one was performed with catalysts of γ-amino alcohols that were synthesized from D-glucose.A linear relationship between the optical yield of this Michael addition and the specific rotat

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