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16850-00-3

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16850-00-3 Usage

Derivation

Derived from benzoic acid and 3-mercaptopropionic acid

Common Uses

Chemical intermediate in organic synthesis
Crosslinking agent in polymer and adhesive production
Production of pharmaceuticals, agricultural chemicals, and fragrances

Odor

Strong odor

Classification

Hazardous material

Importance

Crucial role in various industrial processes and applications

Check Digit Verification of cas no

The CAS Registry Mumber 16850-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,5 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16850-00:
(7*1)+(6*6)+(5*8)+(4*5)+(3*0)+(2*0)+(1*0)=103
103 % 10 = 3
So 16850-00-3 is a valid CAS Registry Number.

16850-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 3-sulfanylpropanoate

1.2 Other means of identification

Product number -
Other names 3-Mercaptopropionic acid benzyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:16850-00-3 SDS

16850-00-3Relevant articles and documents

Poly-6-cationic amphiphilic cyclodextrins designed for gene delivery

Byrne, Colin,Sallas, Florence,Rai, Dilip K.,Ogier, Julien,Darcy, Raphael

, p. 3763 - 3771 (2009)

A new series of amphiphilic cyclodextrins containing cationic groups at the 6-positions and alkyl or biolabile ester groups at the 2-positions has been synthesised. Selective 2-O-allylation followed by photochemical addition of lipophilic thiols made it possible to control lipophilicity in these mesomolecules and allow solubility and self-assembly in water. The cationic groups are cysteamine-derived, while the alkyl and ester groups are C 1-C16 and benzyl ester groups. This is a new general synthetic route to a potentially wide range of polycationic cyclodextrins capable of acting as gene delivery vectors by condensing DNA and forming liquid crystalline complexes with oligonucleotides.

OXIME SULFONATE DERIVATIVES

-

Page/Page column 56, (2016/03/22)

Oxime sulfonate compounds of the formula (I), wherein R 1 is O(CO)R 4, COOR 5 or CONR 6R 7; n is 1 or 2; R 2 for example is C 1-C 8alkyl, C 3-C 6

ORGANIC COMPOUNDS

-

, (2008/06/13)

The present invention relates to compounds of the formula; and their use in therapy.

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