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52605-97-7

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52605-97-7 Usage

Chemical Properties

Yellow Liquid

Uses

2,3-Dimethoxypyridine (cas# 52605-97-7) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 52605-97-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,0 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52605-97:
(7*5)+(6*2)+(5*6)+(4*0)+(3*5)+(2*9)+(1*7)=117
117 % 10 = 7
So 52605-97-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO2/c1-9-6-4-3-5-8-7(6)10-2/h3-5H,1-2H3

52605-97-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Packaging
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  • Detail
  • Alfa Aesar

  • (L19624)  2,3-Dimethoxypyridine   

  • 52605-97-7

  • 1g

  • 331.0CNY

  • Detail
  • Alfa Aesar

  • (L19624)  2,3-Dimethoxypyridine   

  • 52605-97-7

  • 5g

  • 1100.0CNY

  • Detail
  • Alfa Aesar

  • (L19624)  2,3-Dimethoxypyridine   

  • 52605-97-7

  • 25g

  • 3936.0CNY

  • Detail

52605-97-7SDS

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 2,3-Dimethoxypyridine

1.2 Other means of identification

Product number -
Other names 2,3-dimethoxy-pyridine

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:52605-97-7 SDS

52605-97-7Relevant articles and documents

D-AMINO ACID OXIDASE INHIBITORS AND THERAPEUTIC USES THEREOF

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Paragraph 0183, (2019/04/29)

The present invention relates to compounds of Formula (I): or a pharmaceutically acceptable salt thereof, wherein: each of A, B, C, D, and E, independently, is C, N, N—H, O, S, or absent is a single bond or a double bond; each of X, Y, and Z, independentl

FSH RECEPTOR ANTAGONISTS

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Page/Page column 90, (2013/04/10)

The invention relates to FSH receptor antagonist according to general formula (I) or a pharmaceutically acceptable salt thereof and to a pharmaceutical composition containing the same. The compounds can be used for the treatment and prevention of endometriosis, for the treatment and prevention of pre-menopausal and peri-menopausal hormone-dependent breast cancer, for contraception, and for the treatment of uterine fibroids and other menstrual-related disorders

CAMPTOTHECIN-ANALOG WITH A NOVEL, “FLIPPED” LACTONE-STABLE, E-RING AND METHODS FOR MAKING AND USING SAME

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Page/Page column 40-41, (2008/06/13)

The present invention discloses: (i) a novel, lactone-stable, “flipped” E-ring camptothecin, pharmaceutically-acceptable salts, and/or analogs thereof; (ii) methods of synthesis of said novel, lactone-stable, “flipped” E-ring camptothecin, pharmaceutically-acceptable salts, and/or analogs thereof; (iii) pharmaceutically-acceptable formulations comprising said novel, lactone-stable, “flipped” E-ring camptothecin, pharmaceutically-acceptable salts, and/or analogs thereof, and, optionally, one or more additional chemotherapeutic agents; (iv) methods of administration of said novel, lactone-stable, “flipped” E-ring camptothecin, pharmaceutically-acceptable salts, and/or analogs thereof, and, optionally, one or more additional chemotherapeutic agents, to subjects in need thereof; and (v) devices for the administration of said novel, lactone-stable, “flipped” E-ring camptothecin, pharmaceutically-acceptable salts, and/or analogs thereof, and, optionally, one or more chemotherapeutic agents, to subjects in need thereof.

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