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2-thio-β-D-lactosyl benzohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1350982-81-8 Structure
  • Basic information

    1. Product Name: 2-thio-β-D-lactosyl benzohydrazide
    2. Synonyms: 2-thio-β-D-lactosyl benzohydrazide
    3. CAS NO:1350982-81-8
    4. Molecular Formula:
    5. Molecular Weight: 492.504
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1350982-81-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-thio-β-D-lactosyl benzohydrazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-thio-β-D-lactosyl benzohydrazide(1350982-81-8)
    11. EPA Substance Registry System: 2-thio-β-D-lactosyl benzohydrazide(1350982-81-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1350982-81-8(Hazardous Substances Data)

1350982-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1350982-81-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,0,9,8 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1350982-81:
(9*1)+(8*3)+(7*5)+(6*0)+(5*9)+(4*8)+(3*2)+(2*8)+(1*1)=168
168 % 10 = 8
So 1350982-81-8 is a valid CAS Registry Number.

1350982-81-8Downstream Products

1350982-81-8Relevant articles and documents

Molecular design, synthesis and bioactivity of glycosyl hydrazine and hydrazone derivatives: Notable effects of the sugar moiety

Cui, Zining,Yang, Xinling,Shi, Yanxia,Uzawa, Hirotaka,Cui, Jingrong,Dohi, Hirofumi,Nishida, Yoshihiro

, p. 7193 - 7196 (2011)

Assuming that the water solubility of our previous hydrazone derivatives would improve after modification with sugars while keeping or modulating their notable biological activities, we designed and synthesized some glycosyl hydrazine and hydrazone derivatives. Bioassay results indicated that the antitumor activity of our previously prepared hydrazones reduced or disappeared after modification with sugars. On the contrary, some glycosyl derivatives displayed much better antifungal activity against selected fungi. Obviously, a small sugar can change the biological activity of hydrazones significantly.

Molecular design and synthesis of novel salicyl glycoconjugates as elicitors against plant diseases

Cui, Zining,Ito, Jun,Dohi, Hirofumi,Amemiya, Yoshimiki,Nishida, Yoshihiro

, (2015/02/19)

A new series of salicyl glycoconjugates containing hydrazide and hydrazone moieties were designed and synthesized. The bioassay indicated that the novel compounds had no in vitro fungicidal activity but showed significant in vivo antifungal activity against the tested fungal pathogens. Some compounds even had superior activity than the commercial fungicides in greenhouse trial. The results of RT-PCR analysis showed that the designed salicyl glycoconjugates could induce the expression of LOX1 and Cs-AOS2, which are the specific marker genes of jasmonate signaling pathway, to trigger the plant defense resistance.

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