2-DEOXYRIBOSE, D-

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C5H10O4
Molecular Weight	134.1307
Optical Activity	UNSPECIFIED
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 2-DEOXYRIBOSE, D-

Structure Search

SMILES

OC[C@@H](O)[C@@H](O)CC=O

InChI

InChIKey=ASJSAQIRZKANQN-CRCLSJGQSA-N

InChI=1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C5H10O4
Molecular Weight	134.1307
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 17:33:20 GMT 2025` Edited by `admin` on `Mon Mar 31 17:33:20 GMT 2025`
Record UNII	LSW4H01241
Record Status	`FAILED`
Record Version

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Name

Type

Language

2-DEOXYRIBOSE, D-

Common Name

English

D-2-DEOXYRIBOSE

Preferred Name

English

D-(-)-2-DEOXYRIBOSE

Common Name

English

(3S,4R)-3,4,5-TRIHYDROXYPENTANAL

Systematic Name

English

D-2-DEOXYRIBOSE [MI]

Common Name

English

THYMINOSE

Common Name

English

2-DEOXY-D-ERYTHRO-PENTOSE

Systematic Name

English

CLADRIBINE IMPURITY E [EP IMPURITY]

Common Name

English

(4S,5R)-5-(HYDROXYMETHYL)TETRAHYDROFURAN-2,4-DIOL

Systematic Name

English

2-DEOXY-D-RIBOSE

Systematic Name

English

D-ERYTHRO-2-DEOXYPENTOSE

Common Name

English

Code System Code Type Description

CAS

1831121-84-6

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

ALTERNATIVE

ECHA (EC/EINECS)

208-573-0

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

WIKIPEDIA

Deoxyribose

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

CAS

533-67-5

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

PUBCHEM

5460005

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

FDA UNII

LSW4H01241

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

CHEBI

90761

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

CHEBI

27806

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

MERCK INDEX

m4179

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

Merck Index

CAS

35536-75-5

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

ALTERNATIVE

CHEBI

28816

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

EPA CompTox

DTXSID70883428

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

PRIMARY

CAS

452-51-7

Created by admin on Mon Mar 31 17:33:20 GMT 2025 , Edited by admin on Mon Mar 31 17:33:20 GMT 2025

ALTERNATIVE

Related Record Type Details


					47M74X9YT5

PARENT -> IMPURITY

Interaction Type:

CHROMATOGRAPHIC PURITY (TLC)

Qualification:

EP

Amount: