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3992-42-5

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3992-42-5 Usage

Chemical Properties

White crystalline powder

Uses

2''-Deoxycytidine Hydrochloride can be used in methods to produce and use pancreatic endocrine cells.

Check Digit Verification of cas no

The CAS Registry Mumber 3992-42-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,9 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3992-42:
(6*3)+(5*9)+(4*9)+(3*2)+(2*4)+(1*2)=115
115 % 10 = 5
So 3992-42-5 is a valid CAS Registry Number.

3992-42-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (D0048)  2'-Deoxycytidine Hydrochloride  >98.0%(T)

  • 3992-42-5

  • 5g

  • 890.00CNY

  • Detail
  • TCI America

  • (D0048)  2'-Deoxycytidine Hydrochloride  >98.0%(T)

  • 3992-42-5

  • 25g

  • 2,990.00CNY

  • Detail
  • Alfa Aesar

  • (L14153)  2'-Deoxycytidine hydrochloride, 99%   

  • 3992-42-5

  • 250mg

  • 162.0CNY

  • Detail
  • Alfa Aesar

  • (L14153)  2'-Deoxycytidine hydrochloride, 99%   

  • 3992-42-5

  • 1g

  • 449.0CNY

  • Detail

3992-42-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2'-Deoxycytidine hydrochloride

1.2 Other means of identification

Product number -
Other names 2'-Deoxy-D-cytidineHCl

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:3992-42-5 SDS

3992-42-5Relevant articles and documents

An efficient amination method for manufacturing cytidines

Komatsu, Hironori,Morizane, Kunihiko,Kohno, Toshiyuki,Tanikawa, Hiroharu

, p. 564 - 567 (2004)

A novel method for amination of uridine derivatives was developed and applied to the syntheses of cytidines. The method consists of an activation step with 1-methylpiperidine at the C4-position of a uracil base. Large-scale preparation of 2′-deoxycytidine was performed using this method.

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