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107058-94-6

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107058-94-6 Usage

Primary Use

Plasticizer and solvent in industrial processes

Derivation

Derived from 1,3-dioxane-5,5-dimethanol

Structural Features

Contains a phenyl group and two acetate functional groups

Functionality

Improves flexibility and durability of plastic products

Applications

Production of polymers, resins, and coatings

Additional Uses

Solubilizer and emollient in pharmaceutical and personal care products

Environmental Concerns

Potential risks leading to regulations on usage and disposal

Health Risks

Potential risks associated with its use, necessitating careful handling and disposal

Regulatory Status

Subject to regulations due to environmental and health concerns

Check Digit Verification of cas no

The CAS Registry Mumber 107058-94-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,5 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107058-94:
(8*1)+(7*0)+(6*7)+(5*0)+(4*5)+(3*8)+(2*9)+(1*4)=116
116 % 10 = 6
So 107058-94-6 is a valid CAS Registry Number.

107058-94-6SDS

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 acetic acid,[5-(hydroxymethyl)-2-phenyl-1,3-dioxan-5-yl]methanol

1.2 Other means of identification

Product number -
Other names Di-O-acetyl-O-benzyliden-pentaerythrit

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:107058-94-6 SDS

107058-94-6Downstream Products

107058-94-6Relevant articles and documents

Synthesis of functionalised derivatives of pentaerythritol

Ashry, E. S. H. El,Kilany, Y. El,Hamid, H. Abdel,El-Zemity, S. R.,Boghdady, S.

, p. 111 - 128 (2007/10/03)

Ring opening of the dibenzylidene derivative of pentaerythritol 12 with N-bromosuccinimide gave di-O-benzoyldibromodideoxypentaerythritol (29). Reaction of 20 and 21 with hydrogen bromide in acetic acid afforded di-O-acetyl-di-O-p-toluenesulfonyl pentaerythritol (26). Nucleophilic displacement of the tosyloxy groups in 20 by 1,2,4 triazole afforded 2-phenyl-5-(p-toluenesulfonyloxymethyl)-5-(1,2,4-triazolylmethyl)-1,3-dioxan (31) and 2-phenyl-5,5-bis(1,2,4-triazolylmethyl)-1,3-dioxan (32), and with benzotriazole gave 2-phenyl-5,5-bis(benzotriazolylmethyl)-1,3-dioxan (30). The activity of various derivatives against hepatitis B virus has been studied.

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