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7335-65-1

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7335-65-1 Usage

Chemical Properties

white to light yellow adhering crystals or powder

Uses

Different sources of media describe the Uses of 7335-65-1 differently. You can refer to the following data:
1. suzuki reaction
2. Hydrazine acetate has been used in preparation of:2,3,5-tri-O-acetyl-α-L-arabinofuranosyl trichloroacetimidatedisaccharide 4-methoxyphenyl glycoside

Check Digit Verification of cas no

The CAS Registry Mumber 7335-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7335-65:
(6*7)+(5*3)+(4*3)+(3*5)+(2*6)+(1*5)=101
101 % 10 = 1
So 7335-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C2H6N2O2/c1-2(5)6-4-3/h4H,3H2,1H3

7335-65-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Aldrich

  • (259748)  Hydrazineacetate  97%

  • 7335-65-1

  • 259748-5G

  • 734.76CNY

  • Detail
  • Aldrich

  • (259748)  Hydrazineacetate  97%

  • 7335-65-1

  • 259748-25G

  • 2,596.23CNY

  • Detail

7335-65-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Hydrazine acetate

1.2 Other means of identification

Product number -
Other names N2H5(+)*CH3COO(-)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Processing aids, not otherwise listed
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7335-65-1 SDS

7335-65-1Relevant articles and documents

Macrocyclic lactone compound, preparation method thereof, and intermediate application

-

Paragraph 0074; 0075, (2016/10/07)

The invention discloses macrolide compounds with the general structure represented by formula I, a preparation method thereof, an application thereof and an intermediate thereof. The macrolide compounds have very strong activities on most test G bacteria, wherein the activities of two types of compounds to partial gram-positive bacteria are higher than the activities of Azithromycin to the partial gram-positive bacteria.

Synthesis of di- and tri-saccharide fragments of Salmonella typhi Vi capsular polysaccharide and their zwitterionic analogues

Fusari, Matteo,Fallarini, Silvia,Lombardi, Grazia,Lay, Luigi

supporting information, p. 7439 - 7447 (2015/11/27)

Zwitterionic polysaccharides (ZPS) behave like traditional T cell-dependent antigens, suggesting the design of new classes of vaccines alternative to currently used glycoconjugates and based on the artificial introduction of a zwitterionic charge motif onto the carbohydrate structure of pathogen antigens. Here we report the new synthesis and antigenic evaluation of di-/tri-saccharide fragments of Salmonella typhi Vi polysaccharide, as well as of their corresponding zwitterionic analogues. Our strategy is based on versatile intermediates enabling chain elongation either by iterative single monomer attachment or by faster and more flexible approach using disaccharide donors. The effect of structural modifications of the synthetic compounds on antigenic properties was evaluated by competitive ELISA. All the oligosaccharides were recognized by specific anti-Vi polyclonal antibodies in a concentration-dependent manner, and the introduction of a zwitterionic motif into the synthetic molecules did not prevent the binding.

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