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1-(diphenylmethyl)-5-fluoropyrimidine-2,4(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68321-45-9

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68321-45-9 Usage

Type of Compound

Chemotherapy medication

Purpose

Treats various types of cancer

Mechanism of Action

Interferes with the growth and spread of cancer cells in the body

Administration

Commonly administered through injections or infusions

Combination Therapy

Often used in combination with other chemotherapy drugs or treatments

Potency

Potent and effective medication

Side Effects

Potential side effects include nausea, diarrhea, and hair loss

Importance

Crucial component in the treatment of cancer and a vital tool in the fight against the disease

Check Digit Verification of cas no

The CAS Registry Mumber 68321-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,2 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68321-45:
(7*6)+(6*8)+(5*3)+(4*2)+(3*1)+(2*4)+(1*5)=129
129 % 10 = 9
So 68321-45-9 is a valid CAS Registry Number.

68321-45-9SDS

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 1-benzhydryl-5-fluoropyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 1-benzhydryl-5-fluoro-1H-pyrimidine-2,4-dione

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:68321-45-9 SDS

68321-45-9Downstream Products

68321-45-9Relevant academic research and scientific papers

Benzhydryl as an efficient selective nitrogen protecting group for uracils

Wu, Fan,Buhendwa, Musole G.,Weaver, Donald F.

, p. 9307 - 9309 (2007/10/03)

Regioselective N-substitution of the less active nitrogen within uracil analogues has been achieved following preliminary N-protection at the more active N-position with a benzhydryl protecting group. This protecting group is stable to concentrated HCl (a

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